Pharmacovigilance challenges in Biosimilars
Same proportion pharmacovigilance for biosimilars has comparatively more different from other products. Biosimilars 2019 session mainly look that have already been announced to include enhanced tracking and follow-up of post marketing surveillance issues, and on FDA initiative planned different changes in AERS, pilots of new developed post market strategies of drug-monitoring and ADR related problems. The guidelines of biosimilars for pharmacovigilance and pharma epidemiology are the points that shall be laid emphasis in the session In USA average annual income mostly spend on biologics comparing to generic drugs for example:16% on biologics and 3% on other drugs.
- Good pharmacovigilance practice and pharmacoepidemiology
- Detection and evaluation of drug safety signals
- Adverse drug reactions with biologics and biosimilar products
- Current problems in biosimilar pharmacovigilance
- Current problems in biosimilar pharmacovigilance
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Pharmacovigilance challenges in Biosimilars Conference Speakers
Recommended Sessions
- BCS and IVIVC Based on Biosimilars
- Bioequivalence assessment
- Biological Medicine
- Brexit Effect on Biosimilar
- Clinical Development of Biosimilars
- Drug Delivery and Development
- Globalization of Bio Similar
- Intellectual Property Rights
- Pharmacovigilance challenges in Biosimilars
- Analytical Strategies of Biosimilar
- Biosimilars Research Pipeline
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- Current Challenges in Developing Biosimilars
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