DefinitionThis section has been translated automatically.
PRAC is the acronym for "Pharmacovigilance Risk Assessment Committee". This is the committee of the European Medicines Agency (EMA) that is responsible for assessing and monitoring the safety of medicinal products for human use. The committee meets once a month. The EMA publishes the agendas, minutes and highlights of its plenary meetings.
LiteratureThis section has been translated automatically.
- https://www.ema.europa.eu/en/committees/pharmacovigilance-risk-assessment-committee-prac
