Pharmacovigilance Practice
Good pharmacovigilance practices (GVP) are a set of measures drawn up to grease the performance of pharmacovigilance in the European Union (EU). GVP apply to marketing authorisation holders, the European Medicines Agency (EMA) and drugs nonsupervisory authorities in EU Member States. They cover drugs authorised centrally via the Agency as well as drugs authorised at public position. Medicines aren't the only products considered under the horizon of pharmacovigilance practice, but also Vaccines, Blood products, Medical bias, and Biological, Herbals, Traditional / reciprocal substances.
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Pharmacovigilance Practice Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Analysis of Data Quality and Management
- Bio pharmaceutics
- Clinical Database Management
- Clinical Pharmacology
- Clinical Research and Statistics
- Clinical Trials Pharmacovigilance
- Drug development
- Drug Safety
- Ecopharmacovigilance
- Pharmaceutical Chemistry
- Pharmaceutical Nanotechnology
- Pharmacovigilance and Clinical Trials
- Pharmacovigilance Practice
- Regulatory Affairs
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