Pharmacovigilance
The main aim of pharmacovigilance is to provide complete and clear information related to drug safety and various risks and benefits associated with them. Pharmacovigilance can help in providing information of unintended and severe adverse events which could not be provided by clinical trials involving in-vivo method. It enhances the impact of pharmacovigilance on patient welfare and public health and to know what is pharmacovigilance. This track gives a brief discussion on Pharmacovigilance role in healthcare system. Pharmacovigilance legislation gives an outlook on the rules and laws to follow in Pharmacovigilance practice. The Role of pharma industries in the improvement of pharmacovigilance system is very crucial to maintain the safety data, Detection and Evaluation of drug safety signals through manual and medical devices reporting. Pharmacovigilance scope also deals as Ecopharmacovigilance (EPV), pharmacoenvironmentology and pharmacovigilance in herbal medicines.
- Pharmacovigilance systems and their quality systems
- Risk management systems
- Signal management
- Periodic safety update reports
- Good Pharmacovigilance Practice
Related Conference of Pharmacovigilance
February 27-28, 2025
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Prague, Czech Republic
April 07-08, 2025
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Pharmacovigilance Conference Speakers
Recommended Sessions
- Advances In Pharmacological Research
- Adverse Drug Reactions
- Bio and Chemoinformatics
- Bio Availability and Bioequivalence
- Biosimilars & Research Developments
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- Data Integrity in Pharma
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- Drug Delivery Systems & Metabolism
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