Pharmacovigilance and Drug Safety
Pharmacovigilance (PV) is defined as the science and events relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. WHO established that one Programme for International Drug Monitoring in response to the thalidomide disaster detected in 1961.The aims of PV are to enhance patient care and patient safety in relation to the use of medicines.
- Drug safety
- Clinical and preclinical trails
- Bioassay and its types
- Bioassay and its types
- Pharmacovigilance and Risk Management
Related Conference of Pharmacovigilance and Drug Safety
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&
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Pharmacovigilance and Drug Safety Conference Speakers
Recommended Sessions
- Pharmacovigilance and Drug Safety
- Anticancer drug delivery for tumor targeting
- Bioavailability and Bioequivalence
- Biomaterials in Drug Delivery
- Biopharmaceutics and Biologic Drugs
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- Immunotherapy and Vaccines in Drug Delivery
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- Nanomedicine and Nanotechnology
- Novel Drug Delivery Systems
- Peptides and Protein Drug Delivery
- Pharmaceutical Business and Market
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- Pharmaceutical Technology
- Pharmacokinetics and pharmacodynamics in drugs
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