EU Submissions
Reed Tech, the leader in SPL services in the U.S., is monitoring the new requirements for the EudraVigilance Medicinal Product Dictionary (EVMPD) and developing solutions for submissions to the European Medicines Agency (EMA).
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EV Medicinal Product Dictionary
The EMA has launched the first of numerous changes, mandated by the 2010 EU Pharmacovigilance legislation, that are intended to improve patient safety by implementing a risk-based approach to medicinal product management. The EMA now requires the submission…
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