Pharmacovigilance risk management plans
Risk management plan explains the knowledge about the safety and efficacy of a medicinal product. The RMP gives information on plans for studies and other activities to gain knowledge on the safety and efficacy of the medicine. It also describes measures to be undertaken to minimise risks associated with the use of product in patients. Marketing authorisation holders are required to have an RMP for any new medicinal product for human use that must be submitted at the time of application for marketing authorisation. For nationally authorised products RMPs must be submitted for review and approval.
- Risk Minimisation Measures
- Safety communications
- Marketing authorisation
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Pharmacovigilance risk management plans Conference Speakers
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- Regulatory Harmonization & Compliance - Biologics Meet 2026 (UK)
- Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Regulatory Science and Clinical Trial Innovations - Euro Antibiotics 2025 (Netherlands)
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- Risk-Based Monitoring and Trial Optimization - Clinical Trials-2026 (UK)
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- Safety Reporting in Early Phase Trials - Clinical Trials-2026 (UK)
- Semi-Solid Dosage Forms - Formulations 2025 (France)
- Sexually Transmitted Bacterial Infections and Resistance Trends - Euro Antibiotics 2025 (Netherlands)
- Signal Prioritization and Management Techniques - Clinical Trials-2026 (UK)
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- Structure-Based Drug Design and Molecular Docking - Euro MedChem and CADD 2025 (France)
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- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
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- Trending: Digital Health and Telemedicine for Rare Care - ORPHAN DRUGS 2025 (France)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
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- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Women in Rare Disease Leadership and Science - ORPHAN DRUGS 2025 (France)