European Healthcare Distribution Association / Groupement International de la Répartition Pharmaceutique

Draft Legislation

GIRP closely monitors the state of legislation relevant to the pharmaceutical fill-line wholesalers in order to react in a timely and appropriate manner and in order to keep GIRP members informed.

EC Draft Legislation Pharmaceutical Sector

Proposal for a Regulation of the European Parliament and of the Council on in vitro diagnostic medical devices

Proposal for a Regulation of the European Parliament and of the Council on medical devices

Proposal for a Regulation of the European Parliament and of the Council on medical devices - REV 1 COR 1

Proposal for a Regulation of the European Parliament and of the Council on in vitro diagnostic medical devices – ADD1 COR 1

Proposal for a Regulation of the European Parliament and of the Council on in vitro diagnostic medical devices - COR 1

COMMISSION STAFF WORKING DOCUMENT IMPACT ASSESSMENT accompanying the Commission Delegated Regulation (safety features)

COMMISSION STAFF WORKING DOCUMENT EXECUTIVE SUMMARY OF THE IMPACT ASSESSMENT accompanying the Commission Delegated Regulation (safety features)

ANNEXES I to IV to Commission Delegated Regulation (safety features)

Commission Delegated Regulation laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use C(2015)6601

Luxembourg Presidency Proposal for a Regulation of the European Parliament and of the Council on medical devices, and amending Directive 2001/83/EC, Regulation...

Draft legislation

Draft legislation shows proposed legislation that is currently under progress and will have a future impact on the pharmaceutical full-line wholesalers.

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