The European Medicines Agency has proposed significant changes to its pharmacovigilance guideline on risk management plans to further clarify how drug companies should address identified or potential risks of a drug and tackle "missing information" about a product in an RMP. Also, major changes have been proposed to the integrated RMP template1,2.
The changes are the first major revision to the EMA's good pharmacovigilance guideline on RMPs (GVP Module V), which was...
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