[EMA] The European Medicines Agency’s (EMA) committee responsible for assessing and monitoring the safety of human medicines.
Glossary
Pharmacovigilance Risk Assessment Committee (PRAC)
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Take advantage of the knowledge and best practices gained from more than 20 years of research, innovation and development for the health and life sciences sectors.
Glossary
The Life Sciences glossary with terminology, acronyms, for regulatory, quality, compliance, clinical trials, and pharmacovigilance software.
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