Pharmacovigilance
Pharmacovigilance (PV) is defined as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. WHO established its Programme for International Drug Monitoring in response to the thalidomide disaster detected in 1961. Together with the WHO Collaborating Centre for International Drug Monitoring, Uppsala, WHO promotes PV at the country level. At the end of 2010, 134 countries were part of the WHO PV Programme. The aims of PV are to enhance patient care and patient safety in relation to the use of medicines; and to support public health programmes by providing reliable, balanced information for the effective assessment of the risk-benefit profile of medicines.
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Pharmacovigilance Conference Speakers
Recommended Sessions
- Bioorganic Chemistry
- Chemical Synthesis and Catalysis
- Chemo genomics
- Drug Design and Synthesis
- Drug Discovery Chemistry
- Integrating Medicinal Chemistry into the Drug Discovery Process
- Medicinal Chemistry Strategies
- Medicinal Chemistry: Physical Properties and Drug Design
- Medico Marketing
- Nano medicine and Biomedical Applications
- Organic Chemistry
- Pharma Medicinal Chemistry
- Pharmaceutical Formulations: Academic and Industry Perspective
- Pharmaceutical Organic Chemistry
- Pharmaceutical Research and Development
- Pharmacognosy and Phytochemistry
- Pharmacokinetics and Pharmacodynamics in Drugs
- Pharmacovigilance
- Pharmacovigilance and Cosmetovigilance
- Recent Advances in Pharmaceutical Technology
- Solid-state pharmaceutical chemistry
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