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Document C:2006:124:FULL
Official Journal of the European Union, C 124, 25 May 2006
Official Journal of the European Union, C 124, 25 May 2006
Official Journal of the European Union, C 124, 25 May 2006
ISSN 1725-2423 |
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Official Journal of the European Union |
C 124 |
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English edition |
Information and Notices |
Volume 49 |
Notice No |
Contents |
page |
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I Information |
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Council |
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2006/C 124/1 |
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Commission |
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2006/C 124/2 |
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2006/C 124/3 |
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2006/C 124/4 |
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2006/C 124/5 |
Prior notification of a concentration (Case COMP/M.4250 — Industri Kapital/Minimax) — Candidate case for simplified procedure ( 1 ) |
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2006/C 124/6 |
Non-opposition to a notified concentration (Case COMP/M.3968 — Sovion/Südfleisch) ( 1 ) |
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III Notices |
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Commission |
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2006/C 124/7 |
Open call for proposals VP/2006/014 — 2006 — European Year of Workers' Mobility — Pilot Projects |
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Corrigenda |
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2006/C 124/8 |
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(1) Text with EEA relevance |
EN |
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I Information
Council
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/1 |
COUNCIL RECOMMENDATION
of 27 April 2006
on the drawing up of agreements between police, customs and other specialised law enforcement services in relation to the prevention and combating of crime
(2006/C 124/01)
THE COUNCIL OF THE EUROPEAN UNION,
RECALLING that:
(1) |
one of the objectives of the European Union is the progressive establishment of an area of freedom, security and justice by developing common action among the Member States in the field of police and judicial cooperation in criminal matters; |
(2) |
this objective is to be achieved by preventing and combating crime, organised or otherwise, in particular terrorism, trafficking in persons and offences against children, illicit drug trafficking and illicit arms trafficking, corruption and fraud, notably through closer cooperation between police forces, customs authorities and other competent authorities in the Member States, there should also be increased cooperation with, and where appropriate between, EU bodies, Institutions and agencies such as the Commission (OLAF), Europol, Eurojust and Cepol; |
(3) |
the common action provided for by Article 30 of the Treaty on European Union in the field of police cooperation includes operational cooperation between the competent authorities, including the police, customs and other specialised law enforcement services of the Member States in relation to the prevention, detection and investigation of criminal offences; |
(4) |
in order to achieve this objective in the most efficient way, a high degree of cooperation is necessary at national level between the police, customs and other specialised law enforcement services; |
(5) |
the Hague programme on the strengthening of freedom, security and justice in the European Union, adopted by the European Council in November 2004, stressed that an optimal level of protection of the area of freedom, security and justice required multidisciplinary and concerted action both at EU level and at national level between the competent law enforcement authorities, especially police, customs and border guards; |
(6) |
the Commission issued Communications entitled ‘Enhancing police and customs cooperation in the European Union’, ‘Towards enhancing access to information by law enforcement agencies’, and ‘Developing a strategic concept on tackling organised crime’; |
(7) |
different legal and administrative provisions or arrangements exist in Members States on the respective roles and functions of the police forces, customs authorities and other competent authorities in relation to the prevention and combating of crime; |
(8) |
in order to avoid duplication of efforts between police forces, customs authorities and other competent authorities and to make optimum use of their complementary resources, it is essential to promote and ensure a high level of liaison and cooperation, and an effective organisational response; |
(9) |
the Council Resolution of 29 November 1996 on the drawing-up of police/customs agreements in the fight against drugs (1) urged Member States to establish agreements between police and customs services in the fight against drugs, and that the need to extend such agreements to other areas of crime has been recognised, |
HEREBY RECOMMENDS THAT MEMBER STATES:
1. |
take the necessary steps to establish, without prejudice to national legislative and administrative provisions, formal agreements or other arrangements at national level between police forces, customs authorities and other competent authorities in relation to the prevention and combating of crime; |
2. |
incorporate, in these agreements or other arrangements, in particular, provisions covering the following matters:
|
3. |
inform the Council through the General Secretariat within three years of the measures they have taken following this Recommendation; |
4. |
give effect to this Recommendation in replacement of the Resolution of 29 November 1996 on the drawing-up of police/customs agreements in the fight against drugs. |
(1) OJ C 375, 12.12.1996, p. 1.
Commission
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/3 |
Euro exchange rates (1)
24 May 2006
(2006/C 124/02)
1 euro=
|
Currency |
Exchange rate |
USD |
US dollar |
1,2851 |
JPY |
Japanese yen |
143,86 |
DKK |
Danish krone |
7,4563 |
GBP |
Pound sterling |
0,68285 |
SEK |
Swedish krona |
9,3189 |
CHF |
Swiss franc |
1,5509 |
ISK |
Iceland króna |
93,34 |
NOK |
Norwegian krone |
7,8255 |
BGN |
Bulgarian lev |
1,9558 |
CYP |
Cyprus pound |
0,5750 |
CZK |
Czech koruna |
28,210 |
EEK |
Estonian kroon |
15,6466 |
HUF |
Hungarian forint |
263,33 |
LTL |
Lithuanian litas |
3,4528 |
LVL |
Latvian lats |
0,6960 |
MTL |
Maltese lira |
0,4293 |
PLN |
Polish zloty |
3,9602 |
RON |
Romanian leu |
3,5565 |
SIT |
Slovenian tolar |
239,64 |
SKK |
Slovak koruna |
37,850 |
TRY |
Turkish lira |
1,9870 |
AUD |
Australian dollar |
1,7023 |
CAD |
Canadian dollar |
1,4418 |
HKD |
Hong Kong dollar |
9,9667 |
NZD |
New Zealand dollar |
2,0500 |
SGD |
Singapore dollar |
2,0392 |
KRW |
South Korean won |
1 220,33 |
ZAR |
South African rand |
8,5392 |
CNY |
Chinese yuan renminbi |
10,3104 |
HRK |
Croatian kuna |
7,2668 |
IDR |
Indonesian rupiah |
12 054,24 |
MYR |
Malaysian ringgit |
4,681 |
PHP |
Philippine peso |
67,956 |
RUB |
Russian rouble |
34,6500 |
THB |
Thai baht |
49,425 |
Source: reference exchange rate published by the ECB.
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/4 |
Summary of Community decisions on marketing authorizations in respect of medicinal products from 1 April 2006 to 30 April 2006
(Published pursuant to Article 13 or Article 38 of Regulation (EC) No 726/2004 of the European Parliament and of the Council (1))
(2006/C 124/03)
— |
Issuing of a marketing authorization (Article 13 of Regulation (EC) No 726/2004) — Accepted |
Date of the decision |
Name of the medicinal product |
INN (International Non-Proprietary Name) |
Holder of the marketing authorization |
Number of the entry in the Community Register |
Pharmaceutical form |
ATC code (Anatomical Therapeutic Chemical Code) |
Date of notification |
|||||
6.4.2006 |
ProQuad |
Measles, Mumps, Rubella and Varicella Vaccine (Live) |
|
EU/1/05/323/001-011 |
Powder and solvent for suspension for injection |
J07BD54 |
10.4.2006 |
|||||
12.4.2006 |
Omnitrope |
Somatropin |
|
EU/1/06/332/001-003 |
Powder and solvent for solution for injection |
H01AC01 |
20.4.2006 |
|||||
24.4.2006 |
Valtropin |
Somatropin |
|
EU/1/06/335/001 |
Powder and solvent for solution for injection (multi-use) |
H01A C01 |
26.4.2006 |
|||||
24.4.2006 |
Preotact |
Parathyroid hormone |
|
EU/1/06/339/001-002 |
powder and solvent for sol for injection |
H05 AA03 |
26.4.2006 |
|||||
24.4.2006 |
DuoTrav |
Travoprost/Timolol |
|
EU/1/06/338/001-003 |
Eye drops, solution |
S01ED51 |
26.4.2006 |
|||||
24.4.2006 |
Tygacil |
Tigecycline |
|
EU/1/06/336/001 |
Powder for solution for infusion |
(Non applicable) |
26.4.2006 |
— |
Modification of a marketing authorization (Article 13 of Regulation (EC) No 726/2004) — Accepted |
Date of the decision |
Name of the medicinal product |
Holder of the marketing authorization |
Number of the entry in the Community Register |
Date of notification |
||||||||||
3.4.2006 |
Kogenate Bayer |
|
EU/1/00/143/001-006 |
5.4.2006 |
||||||||||
3.4.2006 |
Helixate NexGen |
|
EU/1/00/144/001-003 |
5.4.2006 |
||||||||||
3.4.2006 |
Enbrel |
|
EU/1/99/126/001-011 |
5.4.2006 |
||||||||||
6.4.2006 |
NeuroBloc |
|
EU/1/00/166/001-003 |
10.4.2006 |
||||||||||
6.4.2006 |
Sifrol |
|
EU/1/97/050/001-006 EU/1/97/050/009-012 |
10.4.2006 |
||||||||||
6.4.2006 |
Rapamune |
|
EU/1/01/171/001 EU/1/01/171/007-012 |
10.4.2006 |
||||||||||
6.4.2006 |
Kaletra |
|
EU/1/01/172/001-003 |
10.4.2006 |
||||||||||
6.4.2006 |
Mirapexin |
|
EU/1/97/051/001-006 EU/1/97/051/009-012 |
10.4.2006 |
||||||||||
10.4.2006 |
Trizivir |
|
EU/1/00/156/001-002 |
13.4.2006 |
||||||||||
10.4.2006 |
Zerit |
|
EU/1/96/009/001-009 |
13.4.2006 |
||||||||||
12.4.2006 |
Prevenar |
|
EU/1/00/167/001-007 |
19.4.2006 |
||||||||||
18.4.2006 |
Vaniqa |
|
EU/1/01/173/001-003 |
20.4.2006 |
||||||||||
18.4.2006 |
Orfadin |
|
EU/1/04/303/001-003 |
20.4.2006 |
||||||||||
18.4.2006 |
Telzir |
|
EU/1/04/282/001-002 |
20.4.2006 |
||||||||||
24.4.2006 |
Zavesca |
|
EU/1/02/238/001 |
26.4.2006 |
||||||||||
24.4.2006 |
SonoVue |
|
EU/1/01/177/001-002 |
26.4.2006 |
||||||||||
24.4.2006 |
Xigris |
|
EU/1/02/225/001-002 |
26.4.2006 |
||||||||||
24.4.2006 |
Ammonaps |
|
EU/1/99/120/001-004 |
26.4.2006 |
||||||||||
24.4.2006 |
Trazec |
|
EU/1/01/175/001, EU/1/01/175/004-008, EU/1/01/175/011-015 EU/1/01/175/018-021 |
26.4.2006 |
||||||||||
24.4.2006 |
Starlix |
|
EU/1/01/174/001-021 |
26.4.2006 |
||||||||||
24.4.2006 |
Trisenox |
|
EU/1/02/204/001 |
27.4.2006 |
||||||||||
24.4.2006 |
Zometa |
|
EU/1/01/176/001-006 |
26.4.2006 |
||||||||||
24.4.2006 |
TARGRETIN |
|
EU/1/01/178/001 |
26.4.2006 |
||||||||||
24.4.2006 |
Xolair |
|
EU/1/05/319/001-004 |
26.4.2006 |
||||||||||
27.4.2006 |
Emtriva |
|
EU/1/03/261/001-002 |
2.5.2006 |
||||||||||
27.4.2006 |
Aldara |
|
EU/1/98/080/001 |
2.5.2006 |
||||||||||
27.4.2006 |
Comtess |
|
EU/1/98/082/001-004 |
2.5.2006 |
||||||||||
27.4.2006 |
Rebetol |
|
EU/1/99/107/001-005 |
2.5.2006 |
||||||||||
27.4.2006 |
Axura |
|
EU/1/02/218/001-011 |
2.5.2006 |
||||||||||
27.4.2006 |
Abilify |
|
EU/1/04/276/033-035 |
2.5.2006 |
||||||||||
27.4.2006 |
Lumigan |
|
EU/1/02/205/001-002 |
2.5.2006 |
||||||||||
27.4.2006 |
Ebixa |
|
EU/1/02/219/001-013 |
1.5.2006 |
||||||||||
27.4.2006 |
Levviax |
|
EU/1/01/192/001-005 |
2.5.2006 |
||||||||||
27.4.2006 |
Ketek |
|
EU/1/01/191/001-005 |
2.5.2006 |
||||||||||
27.4.2006 |
Taxotere |
|
EU/1/95/002/001-002 |
4.5.2006 |
||||||||||
27.4.2006 |
Fasturtec |
|
EU/1/00/170/001-002 |
2.5.2006 |
||||||||||
27.4.2006 |
PegIntron |
|
EU/1/00/131/001-050 |
2.5.2006 |
||||||||||
27.4.2006 |
ViraferonPeg |
|
EU/1/00/132/001-050 |
2.5.2006 |
||||||||||
27.4.2006 |
Viraferon |
|
EU/1/99/128/001-037 |
2.5.2006 |
||||||||||
27.4.2006 |
IntronA |
|
EU/1/99/127/001-044 |
2.5.2006 |
||||||||||
27.4.2006 |
Keppra |
|
EU/1/00/146/001-030 |
2.5.2006 |
— |
Issuing of a marketing authorization (Article 38 of Regulation (EC) No 726/2004) — Accepted |
Date of the decision |
Name of the medicinal product |
INN (International Non-Proprietary Name) |
Holder of the marketing authorization |
Number of the entry in the Community Register |
Pharmaceutical form |
ATC code (Anatomical Therapeutic Chemical Code) |
Date of notification |
||||
10.4.2006 |
Flexicam |
Meloxicam |
|
EU/2/06/058/001-003 |
oral suspension |
QM01AC06 |
13.4.2006 |
— |
Modification of a marketing authorization (Article 38 of Regulation (EC) No 726/2004) — Accepted |
Date of the decision |
Name of the medicinal product |
Holder of the marketing authorization |
Number of the entry in the Community Register |
Date of notification |
||||
10.4.2006 |
Porcilis Porcoli |
|
EU/2/96/001/001-010 |
13.4.2006 |
||||
18.4.2006 |
Eurican Herpes 205 |
|
EU/2/01/029/001-003 |
20.4.2006 |
||||
24.4.2006 |
Sevoflo |
|
EU/2/02/035/007 |
26.4.2006 |
Anyone wishing to consult the public assessment report on the medicinal products in question and the decisions relating thereto is invited to contact:
The European Medicines Agency |
7, Westferry Circus, Canary Wharf |
London E14 4HB |
United Kingdom |
(1) OJ L 136 of 30.4.2004, p. 1.
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/11 |
Summary of Community decisions on marketing authorizations in respect of medicinal products from 1 April 2006 to 30 April 2006
(Decisions taken pursuant to Article 34 of Directive 2001/83/EC (1) or Article 38 of Directive 2001/82/EC (2))
(2006/C 124/04)
Issuing, maintenance or modification of a national marketing authorisation
Date of the decision |
Name(s) of the medicinal product |
Holder(s) of the marketing authorization |
Member State concerned |
Date of notification |
3.4.2006 |
Nifedipine |
See Annex I |
See Annex I |
4.4.2006 |
3.4.2006 |
Adartrel |
See Annex II |
See Annex II |
4.4.2006 |
10.4.2006 |
Prograf |
See Annex III |
See Annex III |
12.4.2006 |
(1) OJ L 311, 28.11.2001, p. 67.
(2) OJ L 311, 28.11.2001, p. 1.
ANNEX I
LIST OF THE NAMES, PHARMACEUTICAL FORMS, STRENGTHS OF THE MEDICINAL PRODUCTS, ROUTES OF ADMINISTRATION, APPLICANTS, MARKETING AUTHORISATION HOLDERS IN THE MEMBER STATES
Member State |
Marketing Authorisation Holder |
Applicant |
Name |
Strength |
Pharmaceutical Form |
Route of administration |
||||||
Belgium |
|
|
Nifedipine TEVA 30/60 mg retard |
30 mg/60 mg |
prolonged-release tablets |
Oral use |
||||||
Netherlands |
|
|
Nifedipine Pharmamatch retard 30/60 mg |
30 mg/60 mg |
prolonged-release tablets |
Oral use |
||||||
United Kingdom |
|
|
Neozipine XL 30/60 mg |
30 mg/60 mg |
prolonged-release tablets |
Oral use |
ANNEX II
LIST OF THE NAMES, PHARMACEUTICAL FORM, STRENGTHS OF THE MEDICINAL PRODUCTS, ROUTE OF ADMINISTRATION, APPLICANT, MARKETING AUTHORISATION HOLDER IN THE MEMBER STATES
MMember state |
Marketing authorization Holder |
Applicant |
Invented name |
Strengths |
Pharmaceutical form |
Route of administration |
|||||
Austria |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Austria |
|
Laboratoire GlaxoSmithKline, 100 Route de Versailles, F-78163 Marly-le-Roi Cedex |
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Austria |
|
Laboratoire GlaxoSmithKline, 100 Route de Versailles, F-78163 Marly-le-Roi Cedex |
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Austria |
|
Laboratoire GlaxoSmithKline, 100 Route de Versailles, F-78163 Marly-le-Roi Cedex |
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Belgium |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Belgium |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Belgium |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Belgium |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Cyprus |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Cyprus |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Cyprus |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Cyprus |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Czech Republic |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Czech Republic |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Czech Republic |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Czech Republic |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Denmark |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Denmark |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Denmark |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Denmark |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Estonia |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Estonia |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Estonia |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Estonia |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Finland |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Finland |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Finland |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Finland |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
France |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
France |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
France |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
France |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Germany |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Germany |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Germany |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Germany |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Greece |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Greece |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Greece |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Greece |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Hungary |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Hungary |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Hungary |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Hungary |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Iceland |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Iceland |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Iceland |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Iceland |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Ireland |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Ireland |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Ireland |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Ireland |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Italy |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Italy |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Italy |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Italy |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Latvia |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Latvia |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Latvia |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Latvia |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Lithuania |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Lithuania |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Lithuania |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Lithuania |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Luxembourg |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Luxembourg |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Luxembourg |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Luxembourg |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Malta |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Malta |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Malta |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Malta |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Netherlands |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Netherlands |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Netherlands |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Netherlands |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Norway |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Norway |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Norway |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Norway |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Poland |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Poland |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Poland |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Poland |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Portugal |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Portugal |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Portugal |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Portugal |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Slovakia |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Slovakia |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Slovakia |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Slovakia |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Slovenia |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Slovenia |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Slovenia |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Slovenia |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Spain |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Spain |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Spain |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Spain |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
Sweden |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
Sweden |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
Sweden |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
Sweden |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
|||||
UK |
|
|
ADARTREL |
0,25 mg |
Film-coated tablet |
Oral use |
|||||
UK |
|
|
ADARTREL |
0,5 mg |
Film-coated tablet |
Oral use |
|||||
UK |
|
|
ADARTREL |
1,0 mg |
Film-coated tablet |
Oral use |
|||||
UK |
|
|
ADARTREL |
2,0 mg |
Film-coated tablet |
Oral use |
ANNEX III
LIST OF THE NAMES, PHARMACEUTICAL FORMS, STRENGTHS OF THE MEDICINAL PRODUCT, ROUTES OF ADMINISTRATION, MARKETING AUTHORISATION HOLDERS IN THE MEMBER STATES
Member State |
Marketing Authorisation Holder |
Invented name |
Strength |
Pharmaceutical Form |
Route of administration |
||||||
Austria |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenoius use |
||||||
Austria |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Austria |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Austria |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Belgium |
|
Prograft |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Belgium |
|
Prograft |
1 mg |
Hard Capsules |
Oral use |
||||||
Belgium |
|
Prograft |
5 mg |
Hard Capsules |
Oral use |
||||||
Belgium |
|
Prograft |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Cyprus |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Cyprus |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Cyprus |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Czech Republic |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Czech Republic |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Czech Republic |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Czech Republic |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Germany |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Germany |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Germany |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Germany |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Denmark |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Denmark |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Denmark |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Denmark |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Greece |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Greece |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Greece |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Greece |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Spain |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Spain |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Spain |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Spain |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Finland |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Finland |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Finland |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Finland |
Astellas Pharma a/s Naverland 4 DK-2600 Glostrup |
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
France |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
France |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
France |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
France |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Hungary |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Hungary |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Hungary |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Hungary |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Ireland |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Ireland |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Ireland |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Ireland |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Italy |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Italy |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Italy |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Italy |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Luxembourg |
|
Prograft |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Luxembourg |
|
Prograft |
1 mg |
Hard Capsules |
Oral use |
||||||
Luxembourg |
|
Prograft |
5 mg |
Hard Capsules |
Oral use |
||||||
Luxembourg |
|
Prograft |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
The Netherlands |
|
Prograft |
0,5 mg |
Hard Capsules |
Oral use |
||||||
The Netherlands |
|
Prograft |
1 mg |
Hard Capsules |
Oral use |
||||||
The Netherlands |
|
Prograft |
5 mg |
Hard Capsules |
Oral use |
||||||
The Netherlands |
|
Prograft |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Norway |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Norway |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Norway |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Norway |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Poland |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Poland |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Poland |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Poland |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Portugal |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Portugal |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Portugal |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Portugal |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Slovakia |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Slovakia |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Slovakia |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
Slovenia |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Slovenia |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Sweden |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
Sweden |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
Sweden |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
Sweden |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
||||||
United Kingdom |
|
Prograf |
0,5 mg |
Hard Capsules |
Oral use |
||||||
United Kingdom |
|
Prograf |
1 mg |
Hard Capsules |
Oral use |
||||||
United Kingdom |
|
Prograf |
5 mg |
Hard Capsules |
Oral use |
||||||
United Kingdom |
|
Prograf |
5 mg/ml |
Concentrate for Solution for Infusion |
Intravenous use |
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/32 |
Prior notification of a concentration
(Case COMP/M.4250 — Industri Kapital/Minimax)
Candidate case for simplified procedure
(2006/C 124/05)
(Text with EEA relevance)
1. |
On 17 may 2006, the Commission received a notification of a proposed concentration pursuant to Article 4 of Council Regulation (EC) No 139/2004 (1) by which the undertaking Industri Kapital B.V. acquires within the meaning of Article 3(1)(b) of the Council Regulation control of the whole of the undertaking Minimax Beteiligungs GmbH (‘Minimax’, Germany), controlled by MIMX B.V. (The Netherlands) by way of purchase of shares |
2. |
The business activities of the undertakings concerned are:
|
3. |
On preliminary examination, the Commission finds that the notified transaction could fall within the scope of Regulation (EC) No 139/2004. However, the final decision on this point is reserved. Pursuant to the Commission Notice on a simplified procedure for treatment of certain concentrations under Council Regulation (EC) No 139/2004 (2) it should be noted that this case is a candidate for treatment under the procedure set out in the Notice. |
4. |
The Commission invites interested third parties to submit their possible observations on the proposed operation to the Commission. Observations must reach the Commission not later than 10 days following the date of this publication. Observations can be sent to the Commission by fax (No (32-2) 296 43 01 or 296 72 44) or by post, under reference number COMP/M.4250 — Industri Kapital/Minimax, to the following address:
|
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/33 |
Non-opposition to a notified concentration
(Case COMP/M.3968 — Sovion/Südfleisch)
(2006/C 124/06)
(Text with EEA relevance)
On 21 December 2005, the Commission decided not to oppose the above notified concentration and to declare it compatible with the common market. This decision is based on Article 6(1)(b) of Council Regulation (EC) No 139/2004. The full text of the decision is available only in English and will be made public after it is cleared of any business secrets it may contain. It will be available:
— |
from the Europa competition website (http://ec.europa.eu/comm/competition/mergers/cases/). This website provides various facilities to help locate individual merger decisions, including company, case number, date and sectoral indexes, |
— |
in electronic form on the EUR-Lex website under document number 32005M3968. EUR-Lex is the on-line access to European law. (http://ec.europa.eu/eur-lex/lex) |
III Notices
Commission
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/34 |
OPEN CALL FOR PROPOSALS VP/2006/014
2006 — European Year of Workers' Mobility
Pilot Projects
(2006/C 124/07)
The purpose of the present call for proposals is the co-funding of a limited number of pilot projects in order to:
— |
develop and test innovative instruments which facilitate the geographic and labour market mobility of workers and their families and remove existing obstacles to mobility; |
— |
transfer between sectors, regions and countries or mainstream existing successful instruments and practices in the area of mobility. |
All projects need to evidence a clear European added value and should be able to be reproduced in other contexts. They should involve relevant stakeholders and should have the potential to lead to new policy initiatives.
Proposals must be developed and implemented by a partnership, preferably at transnational level, and must involve at least two relevant stakeholders potentially interested in the objectives of the call (i.e. public authorities and social partner organisations, non governmental organisations, public-private partnerships, academia, municipalities, etc).
The budget available for the present call is EUR 2 million. The Commission will co-finance projects up to a maximum of 85 % of the total eligible costs. Depending on the quality of the applications the Commission expects to fund between 5 and 8 projects (average grant EUR 300 000).
The deadline for the submission of applications is 17.7.2006.
Full information regarding the call for proposals, including the guide for applicants and all relevant documentation can be downloaded at the following address:
http://ec.europa.eu/employment_social/emplweb/tenders/index_en.cfm
Please note that enquiries should be made by e-mail only to:
empl-e-vp/2006/014@ec.europa.eu
Corrigenda
25.5.2006 |
EN |
Official Journal of the European Union |
C 124/35 |
Corrigendum to the communication of the European Centre for the Development of Vocational Training — Publication of the final accounts for the financial year 2004
( Official Journal of the European Union C 269 of 28 October 2005 )
On page 31, table 2, Revenue and expenditure account for the financial years 2004 and 2003 should read as follows:
‘Table 2
Revenue and expenditure account for the financial years 2004 and 2003
(1000 EUR) |
||
|
2004 |
2003 |
Revenue |
||
Commission subsidies |
13 700 |
14 500 |
Revenue from previous financial years |
0 |
0 |
Miscellaneous revenue |
42 |
3 |
Assigned revenue (Phare and third countries) |
724 |
792 |
Financial revenue |
0 |
0 |
Total revenue (a) |
14 466 |
15 295 |
Budgetary expenditure for the financial year |
||
Staff — Title I of the budget |
||
Payments |
8 579 |
7 554 |
Appropriations carried over |
466 |
443 |
Administration — Title II of the budget |
||
Payments |
768 |
778 |
Appropriations carried over |
542 |
358 |
Operating activities — Title III of the budget (except for assigned revenue) |
||
Payments |
2 508 |
2 381 |
Payments on RAL (outstanding commitments)at 31.12.2003 |
2 702 |
|
Appropriations carried over |
0 |
3 138 |
Assigned revenue (Phare and third countries) |
||
Payments |
416 |
546 |
Appropriations carried over |
309 |
246 |
Total expenditure (b) |
16 290 |
15 444 |
Outturn for the financial year (a - b) |
– 1 824 |
– 149 |
Balance carried over from the previous financial year |
– 993 |
– 545 |
Appropriations carried over and cancelled |
56 |
399 |
Neutralisation of the carry-over n-1 in Title 3 linked to the change to differentiated appropriations |
3 138 |
|
Sums for reuse from the previous financial year not used |
1 |
10 |
Refunds to the Commission |
|
– 716 |
Exchange-rate differences |
– 4 |
8 |
Balance for the financial year |
374 |
– 993’ |