Pharmacovigilance and Risk Management
The World Health Organization (WHO) defines pharmacovigilance as the science and activities relating to the detection, evaluation, understanding and prevention of adverse reactions to medicines or any other medicine-related problems. Pharmacovigilance is to protect patients and the public wherever possible and to disseminate knowledge among the relevant professional communities and to patients in order to minimise risk. Pharmacovigilance system or the processes to be engaged in risk management, there is consensus among the major regulators that pharmacovigilance is necessary and important in the development and commercialization of medicinal products.
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- Advanced Pharmaceutical Analysis Techniques
- Applied Pharmaceutical Sciences
- Bioavailability and Bioequivalence Studies
- Challenges in GMP, GCP & Regulatory Affairs
- Clinical Research and Clinical Trials
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- Hospital Pharmacy & Industrial Pharmacy
- Medicinal Chemistry
- Nanotechnology in Pharmaceuticals
- Novel Drug Delivery Systems
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- Pharmacology and new innovations
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