Clinical Trials Pharmacovigilance
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. During clinical trials, the investigator collects and analyzes data on serious adverse events (SAEs), determining whether the drug in question caused the SAEs. If they conclude that the negative side effects were causal, they are categorized as adverse drug reactions (ADRs).
Related Conference of Clinical Trials Pharmacovigilance
May 16-17, 2025
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&
Innovations in Pharma Industry
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Clinical Trials Pharmacovigilance 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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