Pharmacovigilance and Risk Management
Tracks 13: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.
Related Conference of Pharmacovigilance and Risk Management
April 07-08, 2025
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&
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Pharmacovigilance and Risk Management Conference Speakers
Recommended Sessions
- Pharmaceutical Research and Development
- Adverse Drug Reactions
- Causality Assessment
- Clinical Data Management
- Clinical Database Management
- Clinical Research and Statistics
- Clinical Research Nursing
- Clinical Trial Protocols
- Clinical Trials Pharmacovigilance
- Drug Delivery Technologies & Drug Designing and Development
- Drug repurposing to treat Viruses: COVID-19
- Drug Safety
- Drug Safety and Pharmacovigilance
- Global Clinical Trials
- Importance of Audit in Pharmaceutical Industry
- Medical Devices for Drug Delivery
- Pharma Market Research
- Pharmaceutical Nanotechnology: Challenges and Opportunities
- Pharmacoeconomics
- Pharmacokinetics and Pharmacodynamics in Drugs
- Pharmacovigilance and Clinical Trials
- Pharmacovigilance and Cosmetovigilance
- Pharmacovigilance and Risk Management
- Pharmacovigilance Practice
- Pharmacovigilance Significance and Scope
- Prevalence of Potential Drug- Drug Interaction
- Recent trends in Pharma and Technology
- Regulatory Authority Compliance
- Track: 29 Oncology Clinical Research
- Track:30 Risk assessment and management in clinical trials
- Use of Nanoparticles in DDS and Newer Methodologies
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- Stem Cell and Genetic Clinical Research - Clinical Research 2025 (Netherlands)
- Sustainability and Global Health Biotechnology - Biotech-2025 (France)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
- Targeted Drug Delivery and Controlled Release Systems - PHARMA CONFERENCE-2025 (France)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Targeted Therapies in Cardiovascular Regeneration - Cardiovascular-2025 (France)
- Targeting the Renin-Angiotensin-Aldosterone System (RAAS) - Cardiovascular-2025 (France)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Next Generation Approach of Antibiotics - Antibiotics Resistance 2025 (Canada)
- Toxicology - Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
- Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
- Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (France)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (France)