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Should I attach the marketing authorisation application with the risk management plan (RMP, Section 1.8.2 in the registration dossier)?

Since Apr. 2, 2013 there has been an obligation to submit the RMP together with each marketing authorisation application for medicinal products (Section 26, Sub-section 5, Letter l) of the Amendment to AoP), apart from marketing authorisation applications for homeopathic medicinal products and traditional herbal medicinal products.

For marketing authorisation applications in progress it is not necessary to supplement the RMP.