Pharmacovigilance and Risk Management
Pharmacovigilance and Risk Management comprises set of pharmacovigilance activities and interventions designed to identify, characterise, prevent or minimise risks relating to medicinal and therapeutic products including the assessment of the effectiveness of their clinical interventions and combination therapies. Drug industry need to promote companies in pharmacovigilance practice to use information technology and to review softwares used in pharmacovigilance and clinical trials. Monitoring unlicensed, off labels and orphan drugs is major task in risk management. Many experts from different pharmacovigilance CRO’s pharmacovigilance service providers and industrial delegates are participating in this conference to share their knowledge and discuss about the new updates.
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Pharmacovigilance and Risk Management Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Drug Delivery and Design Development
- Drug Delivery Technologies Pharmaceutical Delivery
- Drug Design with the Help of Computers (CADD)
- Drug discovery and Development
- Drug Discovery and Nanotechnology
- Drug Safety
- Forensic Science and Toxicology
- Pharmaceutical Drug Discovery and Nanotechnology
- Pharmacovigilance and Risk Management
- Pharmacy Computer Applications
- Regulatory Affairs
- Research and development in the pharmaceutical industry
- Science of Pharmaceuticals
- The Role of Medicinal Chemistry in Drug Development
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