Pharmacovigilance Crucial for Generic Drug Safety, Including Adverse Event Monitoring

Pharmacovigilance plays a critical role in ensuring the safety and efficacy of generic drugs, according to industry experts. A recent article from DrugPatentWatch highlights the necessity of robust pharmacovigilance systems in the development of generic drugs. The report emphasizes that pharmacovigilance is a critical component of a generic drug’s overall quality and safety profile, as well as a regulatory requirement. The article explains that the generic drug industry often overlooks pharmacovigilance in the rush to market. Generic drug manufacturers are encouraged to prioritize pharmacovigilance from the outset. This includes implementing robust systems for collecting and analyzing adverse event data. Manufacturers should collaborate with regulatory agencies and healthcare professionals to ensure the safe use of generic drugs. Potential consequences of overlooking pharmacovigilance include adverse event reports, product recalls, and damage to a company’s reputation.

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Date: April 14, 2025

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Author

Mark Chiang

紐約 NYU Computer Science 碩士 紐澤西 UMDNJ Biomedical Informatics 博士 中研院博士後 台灣大學博士後