Pharmacovigilance and Clinical Trials
Pharmacovigilance is the wisdom and conditioning relating to the discovery, assessment, understanding and forestalment of adverse goods or any other drug/ vaccine affiliated problem. All drugs and vaccines suffer rigorous testing for safety and efficacy through clinical trials before they're authorized for use. Still, the clinical trial process involves studying these products in a fairly small number of named individualities for a short period of time. Certain side goods may only crop once these products have been used by a miscellaneous population, including people with other concurrent conditions, and over a long period of time.
Related Conference of Pharmacovigilance and Clinical Trials
November 11-12, 2025
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Pharmacovigilance and Clinical Trials 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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