Pharmacovigilance and Drug Safety
The pharmacovigilance is related to collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products, and it is needed in different stages of product life cycle, and the safety surveillance and risk management. Information received from patients and healthcare providers via pharmacovigilance agreements, plays a critical role in providing the data necessary for Pharmacovigilance to take place, in order to market or to test a pharmaceutical product, adverse event data must be submitted to the local drug regulatory authority. Finally pharmacovigilance is concerned with identifying the hazards associated with pharmaceutical products and with minimizing the risk of any harm that may come to patients by safety surveillance and risk management.
Related Conference of Pharmacovigilance and Drug Safety
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Pharmacovigilance and Drug Safety Conference Speakers
Recommended Sessions
- Bioethics and Regulatory Compliance
- Clinical Data Management and Analytics
- Clinical Operations & Project Management
- Clinical Research & Clinical Trials: Academic Perspective
- Clinical Supply Management
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- Clinical Trials on different Diseases
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- Enrollment Planning and Patient Recruitment
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