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Document 52013SC0036
COMMISSION STAFF WORKING DOCUMENT Accompanying the report from the Commission to the European Parliament, the Council and the European economic and social Committee on the implementation of Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 Organisation of market surveillance in the Member States
COMMISSION STAFF WORKING DOCUMENT Accompanying the report from the Commission to the European Parliament, the Council and the European economic and social Committee on the implementation of Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 Organisation of market surveillance in the Member States
COMMISSION STAFF WORKING DOCUMENT Accompanying the report from the Commission to the European Parliament, the Council and the European economic and social Committee on the implementation of Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 Organisation of market surveillance in the Member States
/* SWD/2013/036 final */
COMMISSION STAFF WORKING DOCUMENT Accompanying the report from the Commission to the European Parliament, the Council and the European economic and social Committee on the implementation of Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 Organisation of market surveillance in the Member States /* SWD/2013/036 final */
TABLE OF CONTENTS 1........... INTRODUCTION........................................................................................................ 4 2........... RESPONSES................................................................................................................ 4 2.1........ FRANCE....................................................................................................................... 4 2.2........ UNITED KINGDOM.................................................................................................... 4 2.2.1..... Market Surveillance........................................................................................................ 4 2.2.2..... Customs......................................................................................................................... 5 2.3........ CZECH REPUBLIC...................................................................................................... 6 2.3.1..... Market Surveillance........................................................................................................ 6 2.3.2..... Customs......................................................................................................................... 7 2.4........ FINLAND..................................................................................................................... 8 2.4.1..... Market surveillance......................................................................................................... 8 2.4.2..... Customs......................................................................................................................... 8 2.5........ IRELAND..................................................................................................................... 8 2.5.1..... Market surveillance......................................................................................................... 8 2.5.2..... Customs....................................................................................................................... 11 2.6........ POLAND.................................................................................................................... 11 2.6.1..... Market surveillance....................................................................................................... 11 2.6.2..... Customs....................................................................................................................... 11 2.7........ THE NETHERLANDS................................................................................................ 13 2.7.1..... Market surveillance....................................................................................................... 13 2.7.2..... Customs....................................................................................................................... 13 2.8........ SLOVENIA................................................................................................................. 14 2.8.1..... Market surveillance....................................................................................................... 14 2.8.2..... Customs....................................................................................................................... 14 2.9........ SWEDEN.................................................................................................................... 15 2.9.1..... Market surveillance....................................................................................................... 15 2.9.2..... Customs....................................................................................................................... 16 2.10...... SLOVAKIA................................................................................................................ 16 2.10.1... Market surveillance....................................................................................................... 16 2.10.2... Customs....................................................................................................................... 18 2.11...... GERMANY................................................................................................................. 19 2.11.1... Market surveillance....................................................................................................... 19 2.11.2... Customs....................................................................................................................... 21 2.12...... BULGARIA................................................................................................................. 21 2.12.1... Market surveillance....................................................................................................... 21 2.13...... DENMARK................................................................................................................ 22 2.13.1... Market surveillance....................................................................................................... 22 2.13.2... Customs....................................................................................................................... 22 2.14...... ITALY......................................................................................................................... 22 2.14.1... Market surveillance....................................................................................................... 22 2.14.2... Customs....................................................................................................................... 28 2.15...... LITHUANIA............................................................................................................... 30 2.15.1... Market surveillance....................................................................................................... 30 2.15.2... Customs....................................................................................................................... 31 2.16...... LUXEMBOURG......................................................................................................... 31 2.16.1... Market Surveillance...................................................................................................... 31 2.16.2... Customs....................................................................................................................... 32 COMMISSION STAFF WORKING DOCUMENT Accompanying the report from the Commission to
the European Parliament, the Council and the European economic and social
Committee on the implementation of
Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9
July 2008 setting out the requirements for for accreditation and market
surveillance relating to the marketing of products and repealing
Regulation (EEC) No 339/93
Organisation of market surveillance in the Member States 1. INTRODUCTION Regulation (EC) No 765/2008 establishes
specific requirements for the organisation of market surveillance by Member
States. Most of them have then fine-tuned their administrative structures and
put in place specific solutions to ensure the fulfilment of those requirements.
In view of the preparation of the accompanying report
on the implementation of the Regulation (EC) No 765/2008, the Commission
requested from Member States a contribution regarding the implementation of the
Regulation at national level. This Commission Staff Working Document gives an
overview of the replies of sixteen Member States. The other Member States did
not reply. 2. RESPONSES 2.1. FRANCE France has not
communicated any shortcomings in the market surveillance area. The coordination
between market surveillance authorities is done by the Directorate-General for
Competitiveness and Services (DGCIS), which also centralizes data from
different French authorities monitoring the market to develop the national
market surveillance. It also organizes several annual meetings to exchange
views on the implementation of
Regulation (EC) 765/2008 by different authorities. 2.2. UNITED KINGDOM 2.2.1. Market
Surveillance Before the Regulation (EC) 765/2008 came into
force, Market Surveillance Authorities in UK have already existed and been
indicated for each EU legislation. UK Market Surveillance Co-ordination
Committee was established which includes all UK market surveillance authorities
(and also business interaction). The implementation of ICSMS in all market
surveillance authorities is required. The Regulation has not directly led to any
adjustments to procedures to follow-up complaints, because the UK has had effective systems in place for many years. These systems are reviewed and
amended on a regular basis to ensure that they are fit for purpose e.g.
consumer complaints via Consumer Direct are now made through the Citizens
Advice Bureau which has stronger brand recognition amongst consumers. No adjustments have been made to the existing
systems on procedures to follow-up complaints, to monitor accidents and harm to
health. The UK also continues to feed into the EU’s Injuries Database. UK
believes that a system for the collection of comprehensive accident data is
needed and should be based on the existing EU’s Injuries Database and that
policy decisions to strengthen this (particularly the causal linkages between
accidents and products) and over increased levels of participation needs to be
taken at the Union level. No changes were considered necessary to
strengthen market surveillance authorities' powers, because existing UK enforcement powers are considered to be broadly compatible to those required by the
Regulation. No major adjustments to the UK’s market surveillance system were considered necessary to strengthen market surveillance
authorities' financial and human resources as a direct result of Regulation
(EC) No 765/2008. Measures to avoid multiple inspections and to maintain
competencies of the market surveillance officials will deliver greater
effectiveness and efficiency. Given the current economic climate, public
authority budgets will remain a challenge. Penalties for economic operators have remained
unchanged because UK implementing legislation already meets the relevant
requirements of 765/2008. 2.2.2. Customs A sub-group of the Market Surveillance
Co-ordination Committee has been established involving representatives from the
customs authorities and the market surveillance authorities. This has
established a protocol for the exchange of information and developed policy for
how border controls will be carried out in the UK. The UK has also worked collaboratively with NED
(co-operation project on best practices with the Netherlands (VWA) at their
largest ports (Felixstowe in the UK and Rotterdam in the Netherlands) to develop best practices. A new law has also been made to protect customs
information from misuse when disclosed for the purposes of 765/2008 (SI
2012/1848). The ongoing work is required to ensure that the border controls
work is broadened to cover more points of entry beyond the major container
ports. In addition, the identification of priorities and the management of risk
based profiles is a continuous work in progress to ensure that border controls
are properly targeted and that trade facilitation is not adversely affected.
The main challenges that remain are operational rather than issues revolving
around co-operation. 2.3. CZECH REPUBLIC 2.3.1. Market
Surveillance The responsibility and identity of the CTI (Czech
Trade Inspection) was set out by the Act No. 64/1996 Coll., on the
Czech Trade Inspection, as amended and further responsibilities were identified
by the Act No. 634/1992 Coll., on consumer protection, as amended, Act No.
22/1997 Coll., on technical requirements of products, as amended, Act No.
102/2001 Coll., on general product safety, as amended and by related government
regulations. Act No. 22/1997 Coll. and Act No. 102/2001 Coll. was amended,
namely in relation to the protective measures extension and producers,
importers and distributors obligations. The form of national communication and
co-ordination responsibility setting needs to be introduced. The attribution of responsibilities and the
identity of State Energy Inspection (SEI) authorities were
achieved in Act on business Conditions and Public Administration in the Energy
Sector No. 458/2000 Sb. and in Act on Energy Management No. 406/2000 Sb. in
valid version at the time of entry into force of Regulation 765/2008. SEI was,
on the basis of these two acts, authorized to perform market surveillance on
Energy using Products (EuP). Since 2009 SEI is responsible also for market
surveillance on Energy related Products (ErP), in the field of
implementation Directive 2010/30/EU on the indication by labelling and standard
product information of the consumption of energy and other resources by
energy-related products and Directive 2009/125/EC establishing a framework for
the setting of ecodesign requirements for energy-related products. The attribution of responsibilities and the
identity of Czech Proof House for Arms and Ammunition authorities
were achieved in Act on business Conditions and Public Administration in the
Energy Sector No. 458/2000 Sb. and in Act on Energy Management No. 406/2000 Sb.
in valid version at the time of entry into force of Regulation 765/2008. Communication and coordination between CTI
authorities and between Czech Proof House for Arms and Ammunition
authorities is based on optional mutual agreements only. The communication and
coordination mechanisms between CMA (Czech Mining Authority)
market surveillance authorities were modified by Act No. 490/2009 Coll. Follow-up complaints procedure is set out
sufficiently within the CTI. Accidents and harm to health
monitoring procedure has not been set out in Czech Republic yet. There is a
negotiation between MTI (Ministry of Trade and Industry) and CTI on harm and
health accidents monitoring procedure, therefore an appropriate procedure on
accidents and harm to health needs to be established. In SEI the establishment of
procedure to follow-up complaints was solved in accordance with provision of
the Act on State Inspection No. 552/1991 Sb. and No. 458/2000 Sb. The
complaints are properly checked and if necessary the fines are put on the
account of legal persons according to Administrative Procedure Code No.
500/2004 Sb. SEI is not authorized to inspect and monitor accidents and harm to
health caused by products. Accidents and harm to health monitoring procedure is
not set out yet for Czech Proof House for Arms and Ammunition. The
obligation regarding the procedure to monitor accidents and harm to health has
been already established in CMA. In CTI the financial and human
sources as a whole were reduced due to the budget cut, thus the reorganization
ensured current capacities of human resources. Their goal is to acquire
additional human and financial resources. Strengthening SEI market
surveillance powers is currently enlarged on the base of ongoing implementation
of Directive 2009/125/EC and Directive 2010/30/EU on the different ErP
according to issued Commission Regulations. Strengthening market surveillance authorities'
financial and human resources properly depended and depends on SEI
budget. The ongoing provisions on state budget savings invoke very strict behaviour
for market surveillance activities. Market surveillance goals are ensured with
existing human and financial resources. In CMA, strengthening market
surveillance authorities' powers was adjusted by Act No. 490/009 Coll,
competency ultra vires Act No. 61/1988 Coll and Act No. 552/1991 Coll. In CMA
due to the state budget cut there was no strengthening of market surveillance
authorities' financial and human resources. Effective and dissuasive penalties for economic
operators were established sufficiently for the CTI by relevant
national legislation Act No. 22/1997 Coll. was amended in relation to the
serious and non-serious violation sanctions. SEI is authorized to
put and administrate the penalties during the process of ErP pursuant to listed
act. In CMA, penalties for economic operators were modified by
Act No. 490/2009 Coll – partial extension in comparison with Act No. 61/1988
Coll. 2.3.2. Customs Cooperation between customs and CTI
was set-out by the Act No. 64/1996 Coll. The CTI is represented in the Working
Group on import controls in the area of product safety and compliance,
organised by the Directorate-general Taxation and Customs Union (DG TAXUD) and coordinates
the horizontal cooperation on the national level simultaneously. A number of
agreements between Customs and CTI directorates have been signed. The cooperation between SEI and
customs in the scope of ErP has not been established yet. Cooperation between CMAs and
customs has been already set up by common cooperation (Act No. 500/2004 Coll). 2.4. FINLAND 2.4.1. Market
surveillance Communication and coordination mechanisms
between market surveillance authorities in Finland were adapted by: ·
setting up a working group (NLF-national working
group); ·
the act on the Information Exchange in Market
Surveillance (1197/2009); ·
modifications to the Market Surveillance
Information Exchange Network. Finish authorities are still in preparation of
the general market surveillance programme and in the future they will set up an
official body to carry out coordination tasks. Strengthening of the market surveillance
authorities' powers was adjusted by Section 36 of the Consumer Safety Act
(920/2011) regarding non-compliance related to CE marking. Penalties for economic operators were modified
by the Act on CE marking Infringement (187/2010) and by the Consumer safety Act
(920/2011), Section 52. 2.4.2. Customs Discussions and information exchange are still
ongoing regarding cooperation between market surveillance authorities and
customs. 2.5. IRELAND 2.5.1. Market
surveillance In Ireland responsibilities for sectoral market
surveillance had already been assigned to various market surveillance
authorities through transposition of Directives into national law. Since the Regulation
765/2008 came into force, the Irish Medicines Board (IMB) was nominated as
Competent Authority for cosmetics in October 2010. The role of Market
Surveillance Authority for cosmetics was transferred from the Department of
Health to the IMB in October 2010. A new section on Recreational Craft is being
added to the Marine Survey Office (MSO), section of the Department of
Transport, Tourism and Sports’ (DTTAS) website and updated by the MSO. The IMB
is seeking clarification on need to implement national legislation to formalise
its nomination as the market Surveillance Authority for cosmetics and medical
devices. The system for communication with other market
surveillance authorities is in place which continues to be developed and
enhanced. The IMB has actively participated in the EU working group PEMSAC
(Platform of European Market Surveillance Authorities for cosmetics) since
becoming the Competent Authority for cosmetic products. This group continues to
include improvements on increasing cooperation between market surveillance
authorities within its work programme. Training for GRAS-RAPEX was organised for
Market Surveillance Authorities (MSAs) by the National Consumer Agency (NCA), which
is the national contact point for IT system GRAS-RAPEX[1].Training for ICSMS was
organised for MSAs by the Health & Safety Authority (HSA), the national
contact point for ICSMS. A Market Surveillance Forum (comprised of MSAs
and Customs) meets quarterly to exchange information and to keep abreast of
developments. It is chaired by the Department of Jobs, Enterprise and
Innovation. More specifically, the IMB has established a National Cosmetics
Surveillance Forum consisting of representatives of IMB and Health Service
Executive (HSE) involved in the operational aspects of cosmetic product market
surveillance. The IMB also participates in the European PEMSAC working group
establishing a national work programme on a two-yearly basis. In the medical
devices sector, the IMB is an active participant at the Compliance and
Enforcement Working Group (COEN) and currently holds the position of co-chair
of the Group. Irish authorities still need to ensure that all
projects and activities agreed through SOGS-MSG are communicated to the
relevant directorates-general of the Commission for each sector.(e.g. projects
undertaken by DG TAXUD to be communicated and agreed with DG SANCO for
inclusion into specific annual programme of work for PEMSAC (cosmetics market
surveillance authorities)). Likewise, at the COEN Group, similar challenges
exist to ensure that relevant projects are communicated at a cross-sectoral
level. Procedures for collection of national accident
data in relation to persons at work were already in place. Compliance checks
undertaken have been based on alerts, complaints, inspections and accident
reports. More specifically, the Recreational Craft Directive ADCO Group use
agreed ADM forms (RCDADM) to request information or action from other market
surveillance authorities. Marine Casualty Investigation Board (MCIB) carries
out investigations into marine casualties that take place in Irish waters or
involve Irish registered vessels. Reports are produced on accidents
investigated by the MCIB which include recommendations for appropriate action
to be taken by relevant parties. The IMB manages the medical device vigilance
system for Ireland managing all incidents that occur in Ireland, monitoring all field safety actions in Ireland and taking the lead role in a European
vigilance cases as appropriate. This is all completed in line with Meddev
2.12-1 Guidelines on a medical device Vigilance System. The scope, management
and guidance in the area of medical device vigilance is continuously being
expanded and improved. A new section on Recreational Craft will be
added to the MSO section of the DTTAS website and updated by the MSO – this
will include information on recent relevant RAPEX alerts and follow-up. Marine
Notices are issued where considered relevant on the DTTAS website. Marine
Notices are information notices that are issued to publicise important safety,
regulatory and other relevant information relating to maritime affairs in Ireland. They are circulated to a wide range of individuals and organisations, ranging from
State agencies and the fishing industry, to international shipping and
water-based recreational interests. The IMB has established a cosmeto-vigilance system for
reporting by healthcare professionals and consumers. With the implementation of
Regulation 1223/2009 in July 2013, which introduces mandatory vigilance
reporting requirements for cosmetics, a more formal process will be adopted.
IMB is currently monitoring undesirable effects associated with the use of
cosmetic products. There has been still lack of existing
infrastructure and resources to monitor consumer accidents and harm to health.
The medical devices legislation is currently undergoing a substantial revision
in Europe. It is anticipated that vigilance data will be collated and trend
analysis conducted to detect safety signals sooner. Current cosmetics
legislation does not provide for mandatory reporting requirements (Cosmetics
Directive 76/768/EEC). However with the implementation of Regulation 1223/2009
mandatory reporting requirements are introduced. While Regulation 765/2008 clarifies the powers
for market surveillance authorities, many enforcement powers were already in
place under extant legislation. With the implementation of Regulation 1223/2009
the Competent Authority will have powers to recall and withdraw products posing
a risk to consumers. In the interim solution, the market surveillance authority
only has powers to recall products in case of a serious risk. Irish authorities would like to have in the
future the ability to request those, who place substances, mixtures or articles,
to undertake a product recall. The medical devices legislation is currently
undergoing revision and it is anticipated that proposals will place greater
responsibility on the economic operators within the supply chain. Since 2001 there has been a consistent
increasing trend of market surveillance reports being received, and is
increasing year by year. With the implementation of the new cosmetics
legislation in July 2013 (Regulation 1223/2009) there will be an increase in the
scope for Competent Authorities in terms of monitoring vigilance activities
including increased communication and reporting requirements. Both human and financial resources were
assigned to the extent possible given restrictions and cut-backs in public
sector numbers. Where staff numbers had increased to deal with the work load,
the volume of reports currently being received continues to make this a
challenge to achieve. A risk based approach is currently adopted by the IMB
medical devices section to deal with this challenge. In many cases, an increase in financial and
human resources is not planned due to financial constraints. However, financial
resources are being assigned to cover cost of product testing in respect of
chemical related issues. Increased economic pressures have an impact on
the funding available for market surveillance activities within Ireland. Irish authorities will continue to secure funding for purchase, transport and
testing, especially of complex articles. The IMB is currently investigating the
funding structure for medical devices both at a national and European level.
Optimising funding and resourcing of market surveillance authorities for
medical devices remains a key challenge. A robust funding model based on
periodic fees for surveillance activity may be the best means to secure funding
and allow appropriate development of robust medical device market surveillance
at each national level. In most cases, penalties already existed under
extant legislation. In cosmetics legislation, with the implementation of
Regulation 1223/2009, national implementing provisions will be applied to
address penalties for economic operators. The medical devices legislation is
currently undergoing substantial revision in Europe. This may have an impact on
penalties. 2.5.2. Customs Customs and many market surveillance
authorities have signed Data Exchange Agreements and/or Memoranda of
Understanding (MOU). A Market Surveillance Forum (comprised of MSAs and
Customs) meets quarterly to exchange information and to keep abreast of
developments. It is chaired by the Department of Jobs, Enterprise and
Innovation. The process on signing of MOUs and/or Data
Exchange Agreements between Customs and remaining MSAs is on-going. Training
and development of procedures and the use of check lists is also in progress. In the future Irish authorities would like to
concentrate on co-operation with other market surveillance authorities where
products originate in another EU Member State. Resource challenges are in terms
of inspection including at ports. 2.6. POLAND 2.6.1. Market
surveillance In Poland all minor adjustments were
implemented by the Act of 15 April 2011 on amendments of the conformity
assessment system act and some other acts (OJL of 2011 No. 102, item 586). 2.6.2. Customs Under articles 27-29 of Regulation 765/2008,
customs authorities have the powers to stop import of dangerous/non-compliant
goods and consult relevant competent authorities if import of such goods is in
breach of the legislation on general product safety or conformity of goods.
Accordingly, in Poland: ·
customs authorities contact national competent
authorities in various sectoral fields when they find out that there is a
reason to believe that goods that are placed under customs procedure of release
for free circulation do not fulfill requirements of the relevant legislation; ·
national market surveillance authorities are
obliged to advise customs whether goods mee tthe relevant requirements if their
release for free circulation has been suspended and they should provide their
opinion within three working days; ·
lack of such an opinion means that the goods may
be released for free circulation on condition that they fulfill other relevant
import requirements; ·
in the case of non-compliance, indicated by
market surveillance authorities, customs authorities, if possible, seek
voluntary compliance from an economic operator when a product is found not to
comply with the relevant legislation. However, once a market surveillance
authority (MSA) indicates that it is not possible to apply corrective measures,
customs authorities ban release for free circulation of such products; ·
customs authorities are obliged by national law
to inform the Office of Competition and Consumer Protection, the authority
monitoring the market surveillance system, on actions undertaken with regard to
products which do not meet requirements, i.e. customs authorities inform on the
customs procedure that was assigned to the products, which most often involve re-export
or customs warehouse procedure (if there is a possibility to apply corrective
measures with regard to the product, e.g. labeling, attaching the CE marking); ·
the Polish customs authorities take a risk based
approach in the area of market surveillance checks. Customs officials have
unique access to the documentation relating to imports from third countries,
consequently, the information contained in customs declarations and the
supporting documents is profiled in order to target products that are likely to
present a risk to users. Risk analysis involves a combination of central and
local intelligence. Risk analysis is assisted by electronic customs systems and
RAPEX. Customs authorities co-operate with MSAs,
particularly in the cases of: ·
specific actions, such as joint actions with
other Member States and/or market surveillance authorities (e.g. the PROSAFE
projects on lighters or toys), or ·
a need to implement uniform and/or stricter
measures for a given period of time, or ·
an implementation of a new checklist. In all of the regional customs offices (16
Customs Chambers), there have been designated so called ”co-ordinators for
product safety issues”. These are customs officials who are responsible for
providing assistance to customs officers who perform customs controls,
maintaining contacts with the central authority (Ministry of Finance), carrying
out or assisting in risk analysis, helping to harmonize customs actions, and
training customs officers. A systematic increase in the number of actions
undertaken by customs authorities has been noticed and high efficiency of
customs actions, which is confirmed by a significant number of negative
opinions issued by MSAs. 2.7. THE
NETHERLANDS 2.7.1. Market
surveillance Dutch authorities created a national
coordination platform where all market surveillance authorities (MSAs) in the
field of EU non-food legislation and Customs participate (Alliance group market
surveillance and border controls EU legislation non-foods). Amongst others the
task of this group is to discuss and adopt the Dutch position in the SOGS-MSG
group and in general to improve the information flow, share strategies, tactics
and knowledge (for instance on e-commerce, risk assessment and relations with
Asia) and concrete cooperation between the MSA’s and with customs. In certain domains (e.g. the equipment for
professional use) the current procedure to follow up complaints was improved by
appointing sections/units where a complaint can be filed and investigated by
the inspectorate. For professional products the current
procedure to monitor accidents will be further developed in order to investigate them more systematically.
Priorities were re-organized and resources in
some domains have or are being strengthened. In the future it will be important
to find more financial resources (e.g. by introducing fees for certain
inspections and controls). Penalties for economic operators have been
already established prior to Regulation 765/2008, but in future perspectives
penalties should be increased which will have a more deterrent effect. There is
also a need for more uniformity of penalties. 2.7.2. Customs Several MSAs have established written
agreements with customs to strengthen cooperation in the field of border
controls. These agreements, including roles and responsibilities, differ
depending on the domain in question. Other MSAs are working on improving co-operation
with customs. The future challenge is to enlarge the number
of concrete market surveillance and border controls projects in which a large
number of MSAs and customs authorities participate. There is a need for improving
information sharing between market surveillance and customs authorities as well
as for intensifying cooperation with MSAs of third countries. Another challenging task for the future is
also functioning of the ICSMS system. 2.8. SLOVENIA 2.8.1. Market
surveillance In March 2011 Slovenia adopted new “Act
regulating the technical requirements for products and the conformity
assessment” for designation of the competent market surveillance authorities. The communication and coordination mechanisms
between market surveillance authorities were intensified and strengthened
through existing channels. Ministry of the economic development and technology,
as responsible ministry for the implementation of the Regulation 765/2008, chairs
a “765 Coordinative working group” composed of all market inspectorates and
customs authorities. The work of this group was adjusted to the requirements of
the Article 18 of Regulation 765/2008. There were no changes in the existing Slovenian
system concerning complaints. Slovenia is a member of Injury Data Base (IDB)
since 2006, which includes the injury registries in hospitals. There is no
other systematic monitoring of accidents and harm caused by products. Powers of Slovenian market surveillance authorities
were strengthened through more precise legal base for market surveillance
measures. In March 2011 Slovenian Parliament adopted new “Act regulating the
technical requirements for products and the conformity assessment”. Act for the
purpose of implementing Regulation 765/2008 designates the competent market
surveillance authorities and penal provisions. The entry into force of the Regulation 765/2008
requires strengthening of market surveillance authorities' financial and human
resources. Due to crisis in Slovenia MSAs are not able to earmark more
financial and human resources for more effective implementation. They oriented
all powers for optimisation of the work in the competent market surveillance
authority. Establishment of effective and dissuasive
penalties for economic operators were necessary. This was done through the new
“Act regulating the technical requirements for products and the conformity
assessment”, where chapter IV (Penalties provisions) precisely defines the
level of fine for the offences. 2.8.2. Customs Slovenia reports effective
cooperation between Slovenian Market Surveillance Inspectorate and Slovenian
Customs Office. This cooperation is based on the bilateral agreement between
the Slovenian Market Surveillance Inspectorate and Slovenian Customs Office
(signed in 2003). Since Regulation 765/2008 entered into force, special
agreements for cooperation between market surveillance and customs authorities
are not necessary. Horizontal exchange of information is done through the “765
Coordinative working group” chaired by the Ministry of the economic development
and technology. Sector specific issues are discussed on a bilateral level
between customs authority and different inspectorates. The future challenge is
to strengthen the cooperation between customs authority and other inspectorate
while following the good practice in the case of cooperation between Customs
Office and Market Inspectorate 2.9. SWEDEN 2.9.1. Market
surveillance Responsibilities and identity of authorities
were adapted to Regulation 765/2008 by Law and Regulation on Accreditation and
CE-marking (SFS 2011:791 and SFS 2011:811). Market surveillance provisions
adjusting Swedish law to Regulation 765/2008 have been adopted in some sectors
by: ·
Law and Regulation on explosive products (SFS
2010:1011) and (SFS 2010:1075). ·
Law and Regulation on safety of toys (SFS
2011:579) and (SFS 2011:703). Sweden is in a phase of
adjusting national regulations concerning market surveillance to the Regulation
765/2008. Most Swedish rules concerning responsibilities for market
surveillance are found in national regulations transposing harmonisation
directives (or complementing EU-regulations). Some aspects of market
surveillance are covered by a horizontal regulation (SFS 2005:893), concerning
e.g. cooperation and reporting obligations, which is currently being updated. The future task of Swedish MSA is to update all
Swedish regulations to avoid duplications or even conflicts between national
rules and Regulation 765/2008. In many cases legislation will be updated to
nine directives in the Alignment package. Sweden has had a
coordination body for market surveillance since 2005, designated as the Market
Surveillance Council. Its duties and responsibilities are regulated (e.g. to
establish a national action plan for market surveillance and a yearly report to
the government). The council meets four to five times a year and represents
fifteen MSAs and the Customs. Brand and consumer organisations are invited on a
regular basis and working groups have been established for different issues,
e.g. guidelines for publication of information on dangerous products,
guidelines on how to plan and form the sector specific action plans. In
addition, an external website and an exchange and information system were set
up in 2010 (www.marknadskontroll.se).
The Swedish Agency for Accreditation and Conformity Assessment (Swedac) holds
the secretariat and chairmanship of the Council. The procedure to follow-up complaints, monitor
accidents and harm to health was adapted by Law and Regulation on explosive
products (SFS 2010:1011) and (SFS 2010:1075), Law and Regulation on safety of
toys (SFS 2011:579) and (SFS 2011:703). There is a room for improvements by
using more statistics in order to monitor accidents and a more systematic
approach might be also needed. Powers of market surveillance authorities are
complemented with national legislation which is being updated. Financial
resources for market surveillance are handled as a part of the ordinary Swedish
budgetary process for public authorities. Penalties for economic operators were adapted
to Regulation 765/2008 by: ·
Law and Regulation on explosive products (SFS
2010:1011) and (SFS 2010:1075); ·
Law and Regulation on explosive products (SFS
2010:1011) and (SFS 2010:1075). ·
Law and Regulation on safety of toys (SFS
2011:579) and (SFS 2011:703). The legal support for the duties of MSA (e.g.
penalties/sanctions) varies from sector to sector. All MSAs should have the
same possibilities which will be taken care of when updating national
legislation. 2.9.2. Customs In 2008 a national cooperation model/flowchart
was set up between the Customs and all MSAs. The aim was to clarify the
distribution of responsibilities between Customs and MSAs. Routines for contact
were made between MSAs and Customs. The model was updated to adapt to
Regulation 765/2008. The model is a “living” document and will be updated as a
result of the new DG TAXUD guidelines. In addition, a working group was established
within the Market Surveillance Council in 2011 for all customs related issues. 2.10. SLOVAKIA 2.10.1. Market surveillance Responsibilities and identity of authorities in
Slovakia are governed by the horizontal law[2]
that refers to the specific regulations governing the procedures for the
respective NMSA (supervisory authorities). Responsibilities of STI[3] result
from the Act No.128/2002 Coll. on State control of the internal market in
consumer protection matters, and amending certain laws as amended. Responsibilities of SMA[4] result
from the Act No. 51/1988 Coll. on mining activity, as amended. Responsibilities
of PHA[5]
result from the Act No. 355/2007 Coll. on the protection, promotion and development of public
health and amending certain laws, as amended, and Government Regulation No. 658/2005
Coll. laying down requirements for cosmetic
products, as amended. Responsibilities of SIDC[6] result
from the Act No. 362/2011
Coll. on drugs and medical devices, as amended. Responsibilities
of SMI[7]
result from the Act No. 142/2000 Coll. on metrology, as amended.
Responsibilities of RTRA[8]
result from the Act No. 513/2009 Coll. on railways, as amended.
Responsibilities of TO SR[9]
concerning products covered by the R&TTE and EMC Directive result from the
Act No. 351/2011 Coll. on Electronic Communications (especially article 38, article
36 paragraph 1, article 39 paragraph 2 and article 73), by which the previous
Act No. 610/2003 Coll. was canceled and Act No. 264/1999 Coll. (article 30 and
related articles) on Technical Requirements for Products and on Conformity
Assessment, as amended. Responsibilities of LI[10]
concerning determined products[11]
result from the Act No. 125/2006 Coll. on Labour Inspection, as amended
(amendment of the law with effect from 1.7.2012 in the context of Regulation
765/2008) and Act No. 264/1999 Coll. (article 30 and related articles) on
Technical Requirements for Products and on Conformity Assessment, as amended. There
is a new text of horizontal law on technical requirements for products and on
conformity assessment which should replace the Act. No. 264/1999 Coll.[12] Communication and coordination mechanisms
between market surveillance authorities were created from January 2009 through
inter-departmental Working group (WG), coordinated by SOSMT[13], as the
leader of the implementation of NLF in Slovakia. WG consists of representatives
of the Slovak market surveillance authorities,
relevant ministries and the Custom Department of the Financial Directorate SR. PHI Cooperation Agreement is signed between
the PHI SVFA and STI in the field of control of food and cosmetic products. PHA made
amendment to the Act 355/2007 Coll.[14] There were no major adjustments made concerning
procedure to follow-up complaints. Among other provisions of sectoral
regulations or the horizontal act, there is an Act No. 9/2010 on complaints
which refers to follow-up process of complaints in general. This Act regulates
the procedure for applying, accepting, recording, investigation and written
notification of the result of the investigation of a complaint or its checkup.
No major adjustments were performed to procedure to monitor accidents and harm
to health. In LI complaints are regulated by the Act No. 125/2006
Coll. on Labour Inspection, as amended and Act. No. 124/2006 Coll. on Occupational
Safety and Health. In STI info system ECHO was introduced in
2008. The procedure to follow-up complaints, to monitor
accidents and harm to health of RTRA is set out in article 19 of
the Act No. 513/2009 Coll. on Railways: the operator of the determined
technical equipment[15]
(DTE) is obliged to report to RTRA (Security Authority) the emergence of
incident in operation. In PHI - under "enforcement of preventive
measures in the field of cosmetic products with a particular focus on consumer
education" the procedure for electronic notification of serious adverse
effects of cosmetic products on public health will be developed by the end of
2013. No major adjustments were made regarding strengthening of market surveillance authorities' powers apart from
Safety of toys Directive (2009/48/EC). STI issued a new Act No. 78/2012 Coll. on Safety of toys and on
amending of the Act No. 128/2002 Coll. on State control of the internal market
in consumer protection matters. PHA amended the Act. No. 355/2007 Coll.[16] (Addition of competence in the field of state health supervision in the
field of cosmetic products: impose an obligation for natural or legal person to
take corrective action if product does not comply with the specific regulation,
including withdrawal or recall, impose withdrawal of the product from the
consumer, if product presents a serious risk.). No major adjustments were executed to strengthen market surveillance authorities' financial and human
resources. It is necessary to strengthen market surveillance authorities'
financial and human resources. LI believes that it is necessary to provide funds to verify the safe
condition of the determined product[17],
or clearly define who is required to pay for the costs related to physical and
laboratory tests (under § 7 of the Act No. 125/2006 Coll. on Labour Inspection,
as amended). According to RTRA strengthening of market surveillance
authorities' financial and human resources is required only in case of an
extension beyond the activities carried out so far. No major adjustments were done on penalties for economic operators. Act No. 264/1999 Coll. (article 32)
on Technical Requirements for Products and on Conformity Assessment, as
amended. In RTTA penalties are regulated according to articles
103 and 109 of the Act No. 513/2009 Coll. on Railways, as amended. In PHA
penalties are regulated in amended Act No. 355/2007
Coll. (Change of penalties for natural or legal person depending on the
deficiencies found in the field of cosmetic products.). 2.10.2. Customs Customs Administration SR and NMSA cooperate on
a base of bilateral agreements following the Articles 27-29 of the Regulation
765/2008. Until now cooperation agreements have been
concluded between the Customs Directorate of SR and: ·
Central Inspectorate of the Slovak Trade
Inspection, ·
State Institute for Drugs Control, ·
Department of State Control of Veterinary
Biological Products and Drugs, ·
State Veterinary and Food Administration
of SR. In
STI cooperation Agreements were concluded with the Public Health
Authority SR (control of health safety of toys, childcare products and products
containing the detected volume of chemicals) and the State Veterinary and Food
Administration (control of general food sales requirements). Other cooperation is organised on the basis of
oral agreements and it is applied to case-by-case issues. According to Regulation 765/2008 (articles 27–29),
STI extended "Exchange of information and cooperation within Working group",
coordinated by SOSMT[18]. Negotiations for the conclusion of other
cooperation agreements have already started. PHA made an amendment to the Act 355/2007 Coll.[19] There is also an addition of competencies -
cooperation of public health authorities with the Customs in the area of
inspection of products imported from third countries. The cooperation between different NMSA and the
cooperation with customs still need to be improved. There are two ongoing
projects: the preparation of the opening of the ICSMS
system in Slovakia and training of NMSA in 2013. 2.11. GERMANY 2.11.1. Market surveillance The measures described below refer in the first
line only to market surveillance in the area of the German Product Safety Act
and specified market surveillance activities do not apply to all sectors. This
legal act transposes the General Product Safety Directive and the following
twelve New Approach Directives into German national law: ·
General Product Safety (2001/95/EC), ·
Aerosol dispensers (75/324/EEC), ·
Simple pressure vessels (2009/105/EC), ·
Personal protective equipment (89/686/EEC), ·
Appliances burning gaseous fuels (90/396/EEC), ·
Equipment and protective systems intended for
use in potentially explosive atmospheres (94/9/EC), ·
Recreational craft (94/25/EC), ·
Lifts (95/16/EC), ·
Pressure equipment (97/23/EC), ·
Machinery (2006/42/EC), ·
Low voltage (2006/95/EC), ·
Toys (2009/48/EC), ·
Noise emission in the environment by equipment
for use outdoors (2000/14/EC). ·
The entry into force of the Regulation 765/2008
did not require changes/adjustments in the administrative structure of market
surveillance in the area of the German Product Safety Act. However, as one
result of the MATTEL case (toys recall in 2007) the Federal Government together
with the German Länder (German Federal States) established a programme for the
enhancement of market surveillance (Common
Strategy of the Federal and State Governments to strengthen
market surveillance in the area of the Equipment
and Product Safety Act - http://www.baua.de/de/Produktsicherheit/Marktueberwachung/pdf/Eckpunkte.pdf?__blob=publicationFile&v=1).
One important step in this programme is the attribution of certain enforcement
responsibilities and coordination tasks to the Zentralstelle der Länder für Sicherheitstechnik
–ZLS (Central Authority of the German Federal States for Safety). In special cases (e.g. two or more local market
surveillance authorities involved – diverging risk assessment and therefore
diverging measures) the enforcement competence will pass to the ZLS. The ZLS
could also take over a case by order of the majority of the German Länder.
Changes/adjustments were partially necessary in the area of Energy Efficiency. The
pressure to streamline responsibilities results in the area of energy
labelling, however, rather from the increasing number of covered products and
the increasing workload. As regards communication and coordination,
special tasks were assigned to the ZLS. Changes/adjustments were partially
necessary in the area of Energy Efficiency. In this field a committee on market
surveillance for the coordination between the national level and the level of
the Federal States was established in June 2012. The committee covers market
surveillance in the areas of energy labelling (Directive 2010/30/E) and ecodesign (Directive 2009/125/EC). No special measures were created to the
procedure to follow-up complaints in the area of the German Product Safety Act.
In the area of Energy Efficiency there was a need to establish a procedure on
how to react on notices on non-compliance with energy labelling rules. It was
not necessary to establish a new procedure in terms of administrative law since
existing administrative law covers also administrative decision in terms of
market surveillance activities. No special measures were created for the
procedure to follow-up complaints, to monitor accidents and harm to health in
the area of the German Product Safety Act and also not in the area of Energy
Efficiency, because energy labelling has no effects on product safety and human
health. Since the revision of the Product Safety Act
(entry into force in December 2011), there are provisions for higher fines.
Besides this authorities have to charge economic operators for their testing
and enforcement activities when they find non-compliant products. In the area
of Energy Efficiency, new competences of market surveillance authorities were
introduced, when adapting national energy labelling law to the Regulation
765/2008. Due to the important role of market surveillance
in the area of the German Product Safety Act for both, businesses and
consumers, there is no further staff reduction in this area. In the area of
Energy Efficiency it can only be remarked that financial and human resources of
market surveillance authorities are within the competence of the Länder, not
within the competence at the national level. In the area of Energy Efficiency, resulting
from the additional competences on market surveillance, there are additional
possibilities for penalties. Administrative offences and administrative fines
are, however, no new instruments in the area of energy labelling. 2.11.2. Customs The ZLS will become in 2013 the “contact point”
for the German customs. Nevertheless the cooperation according to articles 27
to 29 of Regulation 765/2008 will still exist at a local level. The guidelines for cooperation between customs
and market surveillance authorities are currently being revised and updated in
the area of the German Product Safety Act. 2.12. BULGARIA 2.12.1. Market
surveillance Communication and coordination mechanisms
between market surveillance authorities were adjusted by Amendments of a Decree
No. 180 of the Council of Ministers from 1 August 2005 for the establishment of
a Council for coordination and exchange of information between market
surveillance authorities. The main aims of the amendments are to clarify the
functions, tasks and the composition of the Council and to move the secretariat
of the Council into the Ministry of Economy, Energy and Tourism. The procedure to follow-up complaints is being
updated. There is a need to develop а procedure/national system to follow-up complaints, to monitor
accidents and harm to health caused by products. 2.13. DENMARK 2.13.1. Market
surveillance There are no major adjustments in
responsibilities and identity of authorities, strengthening of market
surveillance authorities' powers and strengthening of market surveillance
authorities' financial and human resources. Regarding communication and coordination
mechanisms between market surveillance authorities, a market surveillance
committee has been set up to facilitate coordination. Several initiatives on
coordination are ongoing: exchange of experiences on enforcement, including
alternative enforcement mechanisms and formal exchange of officials between
authorities. A main challenge will be to avoid a ‘one size fits all’ approach
but to encompass all authorities in activities in the market surveillance
committee. Denmark improved
procedure to follow-up complaints, monitor accidents and harm to health
following implementation of Regulation 765/2008. A couple of Danish Authorities
already has completed a procedure to follow-up complaints, several authorities
have already set up procedures to monitor accidents and are in the progress of
setting up procedures to monitor harm to health. But there are still a couple
of authorities which have not fully implemented a procedure for monitoring
accident, while others do not deem it relevant. Penalties for economic operators were partly
adjusted to Regulation 765/2008 and as an ongoing process - one authority is currently
changing its penalties. 2.13.2. Customs Some authorities are still in process of
drafting formal cooperation agreements between market surveillance authorities
and customs. Formal cooperation agreement with tax authorities are being
drafted for other authorities. 2.14. ITALY 2.14.1. Market
surveillance Following authorities in Italy contributed to the reply: ·
Ministry of Health,
Department of Public Health and Innovation,
Directorate General for Prevention, REACH Office; ·
Ministry of
Infrastructure and Transport, Port General Command; ·
Department for
Transport, Navigation and Information Systems and Statistics, Directorate
General for Rail Transport; ·
Directorate General for
Maritime and Inland Waterways; ·
Ministry of Economy and
Finance, Independent Administration of State Monopolies (AAMS); ·
Customs agency, Central
Directorate for Verifications and Controls, Office for methodology and control
of trade in the field of customs and taxation; ·
Ministry of Interior,
Department of Public Safety, Office of the General Administration, Affairs
Office of the Social and Administrative Policy; ·
Fire Department of
Public Assistance and Civil Defense, Central Directorate for Prevention and
Technical Safety, Area II - Standardization notification and control; ·
Ministry of Economic
Development, Department of Communications and the Regional Inspectorates,
Directorate General for Planning and spectrum management; ·
Department for
Enterprise Internationalization, Directorate General for industrial policy and
competitiveness; ·
Directorate General for
the Market, Competition, Consumer, Supervisory Board and the Technical
Regulations, Security and Compliance of Products Division; ·
National Union Chamber of
Commerce. 1) Responsibility and identity of authorities: Articles 20 and 50 of the National Decree of 31
March 1998 - attributed to the Chambers of Commerce, Industry,
Crafts and Agriculture the functions performed by the Metric Offices and the
provincial offices for industry, trade and craft (UPICA). This Decree transferred
to the Chamber skills inspections competences, the control of conformity of
products, measurement tools and skills to any sanctions. The aim was to enhance
the role of the chamber as well as to point out the reference for the business
system subject to market regulation, consumer protection and public confidence.
The national legislation of 15 February 2010 re-defined the institutional and
organizational skills of the Chamber of Commerce and the chamber system as a
whole by strengthening the function of supervision and control. The competent
chamber offices comply with the rules of the industry for: ·
Legal metrology; ·
Electrical low voltage;
·
Products subject to
electromagnetic compatibility; ·
Toys; ·
Personal protective
equipment of the first category (eg, sunglasses, ski goggles, etc.); ·
Labeling of footwear; ·
Labeling of textile
products; and in the following aspects: ·
Safety aspects of
products (pursuant to legislative decree of 6 September 2005, No. 206, Part IV,
Title I - articles 102 to 113); ·
Fuel consumption and
emissions of carbon dioxide (CO2) of the various models of new cars; ·
Domestic consumption of
products related to the use of energy. Control activities include the operation
of inspections and sanctions according to the competency of the following: ·
Control of visual
products: these are undertaken by all operators in the industry and are
designed to verify compliance with formal regulations. ·
Controls type of
document on technical dossiers relating to food or metric tools: these checks
are intended to ensure compliance of the products with respect to the technical
requirements laid down by the legislation which is binding and voluntary. ·
Laboratory tests: these
controls are designed to ensure the physical and chemical characteristics of
the products complying with the operation of testing laboratories. The investigative powers of
the Chambers of Commerce are governed not only by the national transposition of
EU directives, but also by national legislation No. 689 of 1981. Ministry of Health: the authorities' control is subject to the enforcement
forum of ECHA ( The European Chemical Agency Helsinki). Ministry of Health, Directorate General for
Prevention: responsibility and identity of
authorities is in accordance with Legislative Decree No. 54/2011, Article 29,
paragraph 5. Supervisory Authority, General Command of
the body of the Harbor - 6th Ward is responsible
for Council Directive 96/98/EC by performing a reacting monitoring (complaints,
specific incidents on board, inspections' national units which issue
certification of ship safety). They check product certification on-board,
perform operational testing on-board and laboratory tests on the product. They
also establish the plan for the activities, cooperate with competent
authorities and have available resources for proactive surveillance. The Ministry of Economic Development, Department
for Enterprise and Internationalization, Directorate General for Market,
Competition, Consumer, Supervision and Technical Regulations, Security and
Compliance Division: article 14 of Legislative Decree 58 of 4 April 2010
implementing Directive 2007/23/EC on the placing on the market of pyrotechnic
products provides supervision to ensure that these items are safe, properly
stored and used for purposes which they are intended for. Ministry of infrastructure and transport,
Department for transport navigation, information systems and statistics,
Directorate-General for maritime transport and inland waterways: the Directive 94/25/EC was amended by Directive 2003/44/EC, which is
implemented by the Legislative Decree No. 171 of 18 July 2005. Article 11,
Paragraph 1 of the Legislative Decree No. 171 provides that the supervisory activities
on recreational craft are carried out in coordination with the Ministry of
Economic Development and the Ministry of Infrastructure and Transport and
within their respective competences. In the legislative context described
above, it should be noted that, with regard to the responsibility of the
Department of Infrastructure and Transport, DG Maritime transport and inland
waterways, the market surveillance of recreational craft is one of the duties
of the Division 5. The performance of office tasks consists of the verification
of conformity of recreational craft and components to the requirements of the
aforementioned Decree, through specific checks and targeted checks on the
market, even with sampling basis (Article 11, paragraph 3) and of the control
of the technical documentation referred to in Annex IX of the Decree, that the
manufacturer or his authorized representative, established in the territory, are
required to keep for ten years (Article 11, paragraph 5). This Office is
working with the relevant sectoral group created in the RCD ADCO for the
preparation of a document "Risk Assessment". Circulation tobacco, Directorate for Excise: Following the correspondence with the Ministry of Economic
Development, this directorate was identified as the authority responsible for
the supervision on fire protection requirements of the cigarettes referred to the
Commission Decision No. 264 of 25 March 2008. 2) Communication and coordination mechanisms between market surveillance
authorities: In order to support
the supervisory activities of the Chambers of Commerce for the
Inspection Campaign National Memorandum of Understanding MED/Unioncamere 2009,
the Information System VIMER was created. VIMER is a database that allows to
record all data of Chambers of Commerce and to report on the inspections
carried out on the field. The data collection and consultation by Chambers and
MED allows monitoring in real time the control activities which are carried out
by the authorities in order to better coordinate the activities throughout the
country in accordance with national surveillance programs and to avoid
duplication in controls. The
system also provides reporting for any notifications in the RAPEX system. In
the VIMER system information is collected and managed on the control activities
carried out by the Chambers of Commerce relating to: Safety of products (toys,
electrical products, personal protective equipment), labeling products (shoes,
textiles) and MID surveillance tools. Ministry of Health: communication and coordination mechanisms
between market surveillance authorities are proceeded through websites and via e-mail. National Administration Ministry of Health,
Directorate General for Prevention created a network
of territorial and central units of NAS (Police Unit for the Protection of health
and safety of products) with the Ministry of Health. The Communication is
provided by electronic mail and paper mail PEC. Circulation
tobacco, Directorate for Excise: Participation in
the seminars for the management of RAPEX and ICSMS platforms. 3) Procedure to follow-up complaints, to monitor accidents and harm to
health: Chambers of Commerce - Information
System VIMER collects, among others, information regarding non-conforming
products and when data are available, it collects also information on
incidents, risk categories and measures taken as a result of the inspection. Ministry of Health: Procedure to follow-up complaints, to monitor
accidents and harm to health exists in Legislative Decree of 9 April 2008 No.
81 on Law safety at workplace. National Administration Ministry of Health,
Directorate General for Prevention established a network
between the Emergency Hospital, the Authorities of territorial control, the
headquarters of Police Unit for the Protection of Health and the Ministry of
Health. Responsible national administration for
Directive 1999/5/EC (Radio and Telecommunications Terminal Equipment) enhance communication with other supervisory authorities (Department of
Business and Internationalization MISE) through representation in the National
Advisory Committee which meets twice per month. Territorial Inspectorates are
involved for products that are potentially harmful to health and results are submitted
to Competent Authority to input data in RAPEX system. 4) Strengthen market
surveillance authorities' powers: Ministry of Health: not
necessary. National Administration Ministry of Health,
Directorate General for Prevention: An agreement signed with
the Region Piemonte: monitoring and evaluation of
the toxicity of cosmetic products and those used in tattoo
parlors, the amount allocated 40,000
EUR. An agreement signed with the Institute ISS: Identification of
volatile organic compounds produced by the combustion of incense on a
scientific basis to promote evaluation and limitations of use, the amount
allocated 55,141,34 EUR. An agreement signed with the National Institute of
Health: Support Action for interventions of Rapid Alert System (RAPEX) and
Remediation of Soils and groundwater which are contaminated, the amount
allocated 250,000 EUR. 5) Strengthen market surveillance authorities' financial and human
resources: in order to strengthen
the supervisory activities of the market surveillance authorities and to adapt
to Regulation 765/2008, the Ministry of Economic Development and Union Chamber
signed in June 2009 a Memorandum of Understanding that provides the allocation
of resources for strengthening of monitoring on the field by the Chambers
of Commerce. The initial term of this protocol has been extended until
31 December 2012. The signature of the new Memorandum of Understanding for the
rest of the activities is an ongoing project. The Protocol provides means to
create a network of services, integrated and in connection with the MED and a
tool that contributes to the creation of a harmonized surveillance system in
the European single market for the benefit of the health and safety of
consumers and the public interests. This plan involved eighty three chambers of
commerce across Italy. Under the Protocol there are also following activities
carried out: ·
Technology Platform for
the national information system that manages controls: an information system
has been set up to collect information on security controls and labeling. The
information system is used to track and manage the control plan at national and
local level and to avoid duplication of controls in this area. ·
Operating procedures
for the conduct of audits: operating procedures and related forms are defined
for each supervision and monitoring arrangement in order to define a common
reference framework for the conduct of audits and facilitate the role of officials
in the chamber and ensure uniformity of behavior in the country. ·
Training of personnel
involved in the activities of the Chamber of Control: general education and
studies on supervisory activities. The training provided useful insights for
the Chamber personnel to carry out the checks in various areas. ·
Communication plan
dedicated to consumers and businesses: the project specific support for
managing information programs directed to the consumer and information/training
directed to economic operators who are potential recipients of control
activities. Ministry of Health: There are currently 220 inspectors on the field for REACH and CLP.
The central surveillance will have about 40 inspectors. The Ministry of Economic Development, Department
for Enterprise and Internationalization, Directorate General for Market,
Competition, Consumer, Supervision and Technical Regulations, Security and
Compliance Division: There are currently
220 inspectors available in the domain of the REACH Regulation and CLP Regulation
(classification, labeling, packaging). In the current situation of economic
difficulty, it is necessary to implement the resources which have not been
adequately sufficient, in order to prepare and ensure that the audit work is
efficient and effective. Circulation tobacco, Directorate for Excise: They have implemented tools and professional resources of the
laboratory of analysis for the implementation of
controls, according to ISO standards, of the fire-prevention requirements of
cigarettes. The Ministry of Economic Development, Department
for Enterprise and Internationalization, Directorate-General for Market,
Competition, Consumer, Supervision and Technical Regulations, Security and
Compliance Division: In this situation of economic difficulty, it is necessary
to implement the resources which have not been adequately sufficient, in order
to prepare and ensure that the audit work is efficient and effective. 6) Penalties for economic
operators: each Chamber of Commerce established an Office for
Penalties for the adoption of sanctions as a result of the administrative
offenses. These offices shall examine the fines
ticket provided by control bodies (Municipal Police, State Police, Finance etc.) for the violation of
standards in various sectors, including security and products' compliances. Ministry of Health: Penalties for economic operator are regulated
by: Legislative Decree No. 133/2009 laying down "Sanctioning discipline
for violation of the provisions of Regulation 1907/2006, which establishes
principles and requirements for registration, evaluation, authorisation and
restriction of chemical substances"; by Legislative Decree 186/2011 laying
down "Discipline penalties for violation of the provisions of Regulation
1272/2008 on the classification, labeling and packaging of substances and
mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and
amending Regulation 1907/2006 "; by Legislative Decree 200/2011 laying
down "Discipline penalties for violation of the provisions of Regulation 689/2008
on the export and import of dangerous chemicals" and by Legislative Decree
266/2006 laying down "Discipline penalties for violation of the provisions
of Regulation 648/2004 on detergents". National Administration Ministry of Health, Directorate
General for Prevention: Penalties for economic
operator are regulated by: Legislative Decree No.
14 of 13 September 2009 (article 16) in relation to violations of Article 67
of REACH Regulation 1907/2006 as amended by
the Regulation 552/2009; by Legislative
Decree No. 54 of 11 April 2011 implementing Directive 2009/48/EC on the safety of toys (article 31) and by Consumer Code
of 6 September 2005 (article 206). The Ministry of Economic Development, Department
for Enterprise and Internationalization, Directorate General for Market,
Competition, Consumer, Supervision and Technical Regulations, Security and
Compliance Division: The rules on penalties are regulated by article 17 of
national legislation No. 58/2010. 2.14.2. Customs Ministry of Health created a monitoring network with all customs ports and airports by
signing the Memorandum of Understanding between the Customs Agency and the
Ministry of Health on 23 March 2007. Control activities are in accordance with articles
27, 28 and 29 of Regulation 765/2008 and the Code of Consumption: ·
Joint projects carried out: "Safe Christmas"
2007, "STOP, Only Safe Toys Please" 2008-2009, Conventions "For
a safer market" 2010-2013, "Safe Toy" 2011-2102 on the strengthening of the audit - when imported - of the
compliance of toys and electrical
products suspected not to satisfy the requirements laid down in Union
legislation on "Updating the procedural manual for customs inspections in
the field of product safety" - December 2009. ·
Joint participation on the preparation of
"Guidelines for import controls in the area of product safety and
compliance", ·
Joint training activities on Directive 2009/48/EC
(Toys Safety Directive) and in cooperation with Assogiocattoli and, in security
and counterfeiting, with National Federation of Electrotechnical and
Electronics (ANIE). ·
Exchange of information for monitoring of market
control activities in the product safety area. ·
Participation in events organized by national
associations. Periodic meetings of coordination on emerging issues. ·
Convention "Secure Toy 2012" on the
strengthening of the audit - import - the compliance of toys and electrical
products suspected of not satisfying the requirements laid down in Union
legislation. ·
Joint actions for the strengthening of the
surveillance of imports of products that may be harmful to the health and
safety of consumers. ·
Joint training activities and seminars. ·
Revision of the procedural manual for customs
inspections in the field of the product safety. The Ministry of Economic Development, Department
for Enterprise and Internationalization, Directorate General for Market,
Competition, Consumer, Supervision and Technical Regulations, Security and
Compliance of Products Division carried out a procedural work for the
realization of the provisions in Tables A and B of the Prime Minister's Decree
No. 242/2010, implementing article 4 of Law 350/2003 on the establishment of a
single customs. National administration responsible for
Directive 1999/5/EC on Radio and Telecommunication Equipment was engaged in a direct exchange with some customs offices to receive news
on non-conforming products and requiring the destination of the product in
order to proceed with further checks involving the competent Territorial
Inspectorates. Ministry of Economic Development Department
for the Enterprise and Internationalization signed
the Convention MISE with Customs Agency ISS-IMQ for Toy Fair 2012 and in
September 2012 they signed the Convention MISE with Customs Agency ISS-IMQ for
Toy Fair 2013-2014. Chambers of Commerce cooperates through specific agreements with other supervisory
authorities (Customs Agency, the Financial Supervision), committed in the area
of the same interests. 2.15. LITHUANIA 2.15.1. Market surveillance 1) Responsibilities and identity of
authorities: There were no major adjustments in all Lithuanian market
surveillance authorities. Responsibilities and identity of authorities are set
out in the following legal acts: ·
Law on the State Labour Inspectorate (Official Gazette,
2008, No. 137-5385). ·
Law on the Weaponry Fund of the Republic of Lithuania under the Ministry of Interior of the Republic of Lithuania (Official
Gazette, 1996, No. 71-1717; 2005, No. 67-2396, 2010 and No. 13-612). ·
Regulation on the State Non Food Products
Inspectorate under the Ministry of Economy (Official Gazette, 2000, No.
53-1558, 2006 and No.14-485). ·
Regulation of the Communications Regulatory
Authority (Official Gazette, 2004, No.131-4734). ·
Regulation of the State Health Care
Accreditation Agency under the Ministry of Health (Official Gazette, 2011, No.
112-5279). ·
Regulation of the Lithuanian Metrology
Inspectorate (Official Gazette, 2011; No. 69-3308). Regulation of the
Lithuanian Maritime Safety Administration (Official Gazette, 2010, 77-3982). 2) Communication and coordination mechanisms
between market surveillance authorities: In 2002 the State Labour
Inspectorate and the State Non Food Inspectorate signed a cooperation
agreement. In 2003 the Communications Regulatory Authority and State Non Food
Products Inspectorate signed a cooperation agreement. 3) Procedure to follow-up complaints,
monitor accidents and harm to health: Lithuanian market surveillance
authorities have internal data bases. The State Non Food Inspectorate and the
State Labour Inspectorate use the RAPEX system for registration and
announcement of dangerous consumer goods. The Lithuanian Maritime Safety
Administration participates in the GRAS-RAPEX system. 4) Strengthen
market surveillance authorities' powers: The powers, which are
granted to Lithuanian market surveillance authorities, are sufficient to
fulfill their functions and tasks described in the legal acts mentioned in
point 1. The provisions regarding strengthening of institution‘s powers will be
foreseen in the Draft of Law on State Labour Inspectorate. 5) Strengthen market surveillance
authorities' financial and human resources: The seminar on CE marking was
held on 15 December 2011. The training on the use of ICSMS took place on 18-20
September 2012. The annual budget of the State Non Food Inspectorate in 2010
was 8.515.000 LTL and 118 people were employed. In 2012 number of personnel was
reduced to 100 and the budget was reduced to 5.228.000 LTL. The annual budget of the Lithuanian Metrology
Inspectorate was reduced from 3.713.000 LTL in 2008 to 2.236.000 LTL in 2012
(number of personnel was reduced from 58 to 43). The
reform of institutions supervising economic entities has been implemented in Lithuania since 2009. The main purpose of the reform is the effectiveness of supervisory
institutions. 6) Penalties for economic operators: The penalty exemption
is foreseen in the Administrative Code (Art. 30(2) of Official Gazette, 1992,
No. 21-610, 2010 and No. 142-7257). 2.15.2. Customs The Agreement on Cooperation between the State
Non Food Products Inspectorate and the Customs was signed in 2002. The
Agreement on Cooperation between the Communications Regulatory Authority and
the Customs was signed in 2003. The Agreement on Exchange of Data between the
State Non Food Products Inspectorate and the Customs was signed in 2004. The Lithuanian Metrology Inspectorate provides
the Customs with the relevant information. The Agreement on Cooperation between the Lithuanian
Maritime Safety Administration and the Customs is under the consideration. The Agreement on Cooperation between the State
Health Care Accreditation Agency under the Ministry of Health and Customs is
under the consideration. 2.16. LUXEMBOURG 2.16.1. Market Surveillance The authorities in Luxembourg are clearly
identified and their responsibilities are defined. However a new law on the
restructuring of ILNAS[20]
foresees some changes in the responsibilities and identity of these
authorities. The State Council has expressed its advice and the Ministry of
Economy and Foreign trade is now waiting that the Parliament will start to work
on the document. The law of 20 May 2008 on the creation of ILNAS
puts in place a communication and coordination structure. A national committee
was created under the responsibility of ILNAS. The new law on the restructuring of ILNAS
clearly covers the procedure to follow-up, to monitor accidents and harm to
health. The ILNAS law of 20 May 2008 covers the
obligation on strengthening of market surveillance authorities' powers. The new
legislation on the restructuring of ILNAS is also strengthening the
authorities’ power. At the moment a new legislation is on the way
regarding strengthening of market surveillance authorities' financial and human
resources. It will reinforce ILNAS’ human resources. Personnel and financial
reinforcement of the market surveillance department is an ongoing challenge. The ILNAS law of 20 May 2008 covers the
penalties for economic operators. The new legislation on the restructuring of
ILNAS will strengthen this obligation, after its adoption. 2.16.2. Customs A cooperation agreement, signed between market
surveillance authorities, has been in place since 1998. To be in line with the Regulation
765/2008, the agreement was amended in 2011. [1] General Rapid Alert System used for the Member states
to submit RAPEX notifications. GRAS-RAPEX replaced the old IT system RAPEX-REIS
and extended the scope of RAPEX to professional products and to other risks
than health and safety. [2] Act No. 264/1999 Coll. on
technical requirements for products and on conformity assessment as amended [3] STI - Slovak Trade Inspection [4] SMA - State Mining Authority [5] PHA - Public Health Authority of SR [6] SIDC - State Institute for Drugs Control [7] SMI - Slovak Metrology Inspection [8] RTRA - Railways Transport Regulation Authority [9] TO SR - Telecommunication Office SR [10] LI - Labour Inspectorates [11] Determined products are such
products that represent higher risk of jeopardy to justified concern [12] Act No. 264/1999 Coll. on
technical requirements for products and on conformity assessment as amended [13] SOSMT - Slovak Office of Standards, Metrology
and Testing [14] Act. 355/2007 Coll. on protection,
promotion and development of public health and amending certain laws under
preparation [15] Determined technical equipment
is such equipment that represent higher risk of jeopardy to justified concern
(Act. No. 264/1999 Coll.) [16] Act No. 355/2007 Coll. on
protection, promotion and development of public health and amending certain
laws under preparation [17] Determined product is such product
that represent higher risk of jeopardy to justified concern (Act No. 264/1999 Coll.)
[18] SOSMT - Slovak Office of Standards,
Metrology and Testing [19] Act No. 355/2007 Coll. on
protection, promotion and development of public health and amending certain
laws [20] Institut luxembourgeois de la normalisation, de l'accréditation, de la
sécurité et
qualité des produits et services.