Risk Management
Pharma Risk Management was desgined as a set of pharmacovigilance activities and interventions designed to identify, characterise, prevent or minimise risks of medicinal and therapeutic products including the assessment of the effectiveness of their clinical reactions, interventions and combination therapies. Drug industry need to promote companies in pharmacovigilance practice to use information technology and provide efficient softwares to implement the risk minimisation plans in drug development and manufacture . Pharmaceutical risk management monitors unlicensed, off labels and orphan drugs ,risk management labeling, regulatory decisions, legal protection, intellectual property, enforcement, marketing, and company reputation.
- Information Technology in Pharmacoepidemiology and Clinical Trials
- Review of Softwares used in Pharmacovigilance and Clinical Trials
- Risk Communication: Interface between Pharmaepidemiology, Sales and Marketing
- Monitoring Unlicensed, off labels and Orphan Drugs
- Implementation of Risk Minimization Plans
- Therapeutic Drug Management
Related Conference of Risk Management
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Risk Management Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Entrepreneurs Investment Meet
- Case Reports in Clinical Trials
- Clinical Data Management
- Clinical Drug Development
- Clinical Pharmacology and Therapeutics
- Clinical Pharmacy
- Diversity in Industrial Clinical Research
- Drug Safety and Pharmacotherapy
- Genetic Epidemiology
- Pharmacoepidemiology and Clinical Research
- Pharmacokinetics and Pharmacodynamics
- Pharmacology
- Pharmacovigilance and its Significance
- Pre-Clinical and Clinical Trials
- Regulatory Affairs
- Risk Management
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