On Tuesday 3 October, MEP Pernille Weiss (EPP, Danish) submitted her draft report amending the proposed directive on pharmaceutical products. It will shortly be discussed by the European Parliament’s Environment Committee.
This directive contains all the requirements for authorisation, monitoring, labelling and regulatory protection, marketing and other regulatory procedures for all medicines authorised at EU level (see EUROPE B13201A23).
The draft report by Tiemo Wölken (S&D, German)...