Medical treatment on board vessels
Seagoing vessels are workplaces which, because of geographical isolation, present heightened risks to the safety and health of workers on board. Vessels should have adequate facilities, regularly checked, so that workers can obtain the necessary medical treatment at sea.
ACT
Council Directive 92/29/EEC of 31 March 1992 on the minimum safety and health requirements for improved medical treatment on board vessels
SUMMARY
WHAT DOES THIS DIRECTIVE DO?
It aims to ensure minimum safety and health systems are in place to improve medical treatment on board vessels.
KEY POINTS
Each EU country should ensure that vessels registered in that country, or flying its flag, carries medical supplies. The detailed requirements depend on the category of vessel and the details listed in the annexes to the directive. In addition:
Any vessel transporting dangerous substances must carry appropriate antidotes. Ferries must in any case carry a minimum of antidotes (as outlined in Annex II) to allow for the fact that the carrying of dangerous substances may not be known in advance unless the regular crossing is under two hours. All available antidotes must be detailed on a checklist.
The owner is responsible for providing the medical supplies. The captain, or a delegated representative, is responsible for the management of supplies, which must be kept in good condition and replenished systematically at the owner’s sole expense.
The medical supplies must be accompanied by instructions as to their use, including information relating to the use of the required antidotes.
Professional maritime training must include basic first response medical training in the event of an accident or serious medical emergency. The captain, or the delegated worker responsible for medical supplies, must receive special training at least every five years.
Centres must be designated to provide workers with free medical advice by radio, including from doctors trained in the special conditions prevailing on board ship.
EU countries must ensure that annual inspections are carried out to check that medical supplies comply with the directive.
WHEN DOES THE DIRECTIVE APPLY?
It came into force on 10 April 1992.
BACKGROUND
Following the COVID-19 outbreak and introducing measures to cope with the impact of the crisis, the European Commission adopted:
REFERENCES
Act |
Entry into force |
Deadline for transposition in the Member States |
Official Journal |
Directive 92/29/EEC |
10.4.1992 |
31.12.1994 |
Amending act(s) |
Entry into force |
Deadline for transposition in the Member States |
Official Journal |
Regulation (EC) No 1882/2003 |
20.11.2003 |
- |
|
Directive 2007/30/EC |
28.6.2007 |
31.12.2012 |
|
Regulation (EC) No 1137/2008 |
11.12.2008 |
- |
Successive amendments and changes to Directive 92/29/EEC have been incorporated in the original text. This consolidated version is of documentary value only.
last update 08.05.2020