Pharmacovigilance and Clinical Trials
The purpose of pharmacovigilance is to enhance patient care and patient safety in relation to the use of medicines according to the life cycle of a health product. Current pharmacovigilance is predominantly based on spontaneous reporting and is mainly helpful in detecting type B effects (those effects that are often allergic or idiosyncratic reactions, characteristically occurring in only a minority of patients and usually unrelated to dosage and that are serious, unexpected
Related Conference of Pharmacovigilance and Clinical Trials
February 27-28, 2025
8th International on Pharmacy and Pharmaceutical Conference
Prague, Czech Republic
April 07-08, 2025
4th International Conference and Expo on Pharmaceutics & Novel Drug Delivery Systems
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17th International Conference on Pharmaceutical Education and Practice
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31st International Conference on Advanced Clinical Research and Clinical Trials
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18th International Conference and Exhibition on Pharmacovigilance & Drug Safety
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Pharmacovigilance and Clinical Trials Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Analysis of Data Quality and Management
- Biopharmaceutics
- Causality Assessment
- Clinical Database Management
- Clinical Trial Protocols
- Clinical Trials Pharmacovigilance
- Global Clinical Trials
- Orphan drugs
- Pharmaceutical Chemistry
- Pharmaceutical Nanotechnology
- Pharmacokinetics
- Pharmacovigilance and Clinical Trials
- Pharmacovigilance Practice
- Regulatory Affairs
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