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8th EGA Pharmacovigilance Discussion Forum 14th EGA Regulatory and Scientific Affairs Conference Reservation Form for: Ref 150118EGMA GUEST INFORMATION: NAME: COMPANY: ADDRESS: CITY: COUNTRY: POST
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What is 8 ega pharmacovigilance discussion?
8 ega pharmacovigilance discussion is a meeting organized by the European Generic and Biosimilar Medicines Association (EGA) to discuss pharmacovigilance issues related to generic and biosimilar medicines.
Who is required to file 8 ega pharmacovigilance discussion?
Marketing authorization holders (MAHs) of generic and biosimilar medicines are required to file 8 ega pharmacovigilance discussion.
How to fill out 8 ega pharmacovigilance discussion?
To fill out 8 ega pharmacovigilance discussion, MAHs need to compile and submit safety data and reports on their products to the EGA.
What is the purpose of 8 ega pharmacovigilance discussion?
The purpose of 8 ega pharmacovigilance discussion is to ensure the safety and efficacy of generic and biosimilar medicines through collaborative pharmacovigilance efforts.
What information must be reported on 8 ega pharmacovigilance discussion?
Information that must be reported on 8 ega pharmacovigilance discussion includes adverse drug reactions, medication errors, and any other safety-related data.
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