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EMA Risk Management Information Day 15 June 2021 13:30 17:30 CEST Virtual EventPROGRAMME COMMITTEE Sabine Strauss Chair of Pharmacovigilance Risk Assessment Committee (PRC) Medicines Evaluation Board
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EMA information data on is information relating to a specific topic gathered and reported by the European Medicines Agency.
Companies and organizations involved in the pharmaceutical industry may be required to file EMA information data on.
EMA information data on can be filled out online through the European Medicines Agency's official website or through submission portals provided by the agency.
The purpose of EMA information data on is to ensure transparency, quality, and safety in the pharmaceutical industry.
Information such as clinical trial data, safety reports, pharmacovigilance data, and marketing authorization updates may need to be reported on EMA information data on.
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