Pharmacovigilance in Clinical Trials
Pharmacovigilance involves ongoing monitoring of drug safety, recording adverse effects during trials, and reporting them to regulatory bodies. This discipline protects patients and informs treatment adjustments, ensuring trial integrity and regulatory compliance. Effective pharmacovigilance reduces patient risk and enhances drug safety profiles.
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Pharmacovigilance in Clinical Trials Conference Speakers
Recommended Sessions
- Adaptive Trial Design
- Informed Consent Process
- Intellectual Property in Clinical Trials
- Phases of Clinical Trials
- Precision Medicine and Biomarker Discovery
- Risk-Based Monitoring (RBM)
- Advances in Patient-Centric and Precision Clinical Trials
- Adverse Event Monitoring and Safety
- Biostatistics and Data Analysis
- Clinical Trial Diversity and Inclusion
- Clinical Trial Logistics and Supply Chain Management
- Contract Research Organizations (CROs)
- Data Collection and Management
- Data Monitoring Committees (DMCs)
- Decentralized and Hybrid Clinical Trials
- Electronic Health Records (EHR) Integration
- Good Clinical Practice (GCP) Standards
- Investigator Training and Responsibilities
- Machine Learning and Artificial Intelligence in Clinical Trials
- Patient Recruitment and Retention
- Patient-Centric Approaches in Clinical Trials
- Patient-Reported Outcomes (PROs)
- Pharmacovigilance in Clinical Trials
- Placebo-Controlled Studies
- Post-Marketing Surveillance and Phase IV Trials
- Quality Assurance (QA) in Clinical Trials
- Randomization in Trials
- Real-World Evidence (RWE) and Real-World Data (RWD)
- Recent Innovations in Pharmaceutical Technology
- Regulatory Compliance and Ethics
- Site Selection and Management
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- Phases of Clinical Trials - Clinical Trials Congress-2026 (France)
- Phytochemistry - Naturalproducts 2026 (UAE)
- Placebo-Controlled Studies - Clinical Trials Congress-2026 (France)
- Post-Marketing Surveillance and Phase IV Trials - Clinical Trials Congress-2026 (France)
- Post-Marketing Surveillance and Real-World Data - Clinical Trials-2026 (UK)
- Pre-clinical and Clinical Trails - Pharmacology 2026 (Italy)
- Pre-Clinical and Clinical Trials - PHARMACOVIGILANCE 2026 (Italy)
- Precision Medicine and Biomarker Discovery - Clinical Trials Congress-2026 (France)
- Psychological and Behavioural Pain Interventions - Pain Management 2026 (France)
- Psychopharmacology & Behavioral Science - Euro Pharmacology 2026 (France)
- Public Health Approaches to Pain Management - Pain Management 2026 (France)
- Purpose and Principles of GMP - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Quality Assurance (QA) in Clinical Trials - Clinical Trials Congress-2026 (France)
- Quality Assurance, GMP & Biotech Manufacturing Excellence - PHARMA BIOTECH 2026 (UK)
- Quantum Chemistry and Molecular Simulations - Euro MedChem and CADD 2026 (France)
- R&D Advancement: Road to New Medicines - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Randomization in Trials - Clinical Trials Congress-2026 (France)
- Real-Time Safety Data Monitoring Strategies - Clinical Trials-2026 (UK)
- Real-World Evidence (RWE) and Real-World Data (RWD) - Clinical Trials Congress-2026 (France)
- Real-World Evidence in Clinical Trials - Pharma Europe 2026 (UK)
- Real-World Evidence in Clinical Trials - Clinical Research 2026 (UK)
- Recent Advances in Pharmacology and Toxicology - Pharmacology 2026 (Italy)
- Recent Innovations in Pharmaceutical Technology - Clinical Trials Congress-2026 (France)
- Regenerative Medicine & Stem Cell Applications - Biotech-2026 (France)
- Regenerative Therapies and Stem Cells - Pain Management 2026 (France)
- Regulatory Affairs & Drug Approval Pathways - Euro Pharmacology 2026 (France)
- Regulatory Affairs & Global Approval - Biologics Meet 2026 (UK)
- Regulatory Affairs and Quality Assurance - Drug-Delivery-2026 (France)
- Regulatory Compliance and Ethics - Clinical Trials Congress-2026 (France)
- Regulatory Harmonization & Compliance - Biologics Meet 2026 (UK)
- Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Regulatory Strategies & Quality Control in Biopharma - Biotech-2026 (France)
- Regulatory updates on Biosimilars - Eurobiosimilars 2026 (Italy)
- Regulatory, Quality Control, and Translational Aspects - Drug Devilvery 2026 (France)
- Rehabilitation and Physical Therapy in Pain - Pain Management 2026 (France)
- Risk-Based Monitoring (RBM) - Clinical Trials Congress-2026 (France)
- Risk-Based Monitoring and Trial Optimization - Clinical Trials-2026 (UK)
- Role of Gut Microbiome in Cardiovascular Health - Cardiovascular-2026 (France)
- Role of Inflammation in Cardiovascular Diseases - Cardiovascular-2026 (France)
- Safety Pharmacology - Pharmacology 2026 (Italy)
- Safety Reporting in Early Phase Trials - Clinical Trials-2026 (UK)
- Semi-Solid Dosage Forms - Formulations 2026 (UK)
- Signal Prioritization and Management Techniques - Clinical Trials-2026 (UK)
- Single-Use Technologies in Production - Biologics Meet 2026 (UK)
- Site Management Innovation - Clinical Research 2026 (UK)
- Site Selection and Management - Clinical Trials Congress-2026 (France)
- Smart Drug Delivery Systems - Pharmatech 2026 (USA)
- Smart Drug Delivery Systems - PHARMACEUTICA 2026 (UK)
- Smart Drug Delivery Systems - Formulations 2026 (UK)
- Smart Polymers and Biomaterials - Drug-Delivery-2026 (France)
- Solid Dosage Forms - Formulations 2026 (UK)
- Stem Cell and Genetic Clinical Research - Clinical Research 2026 (UK)
- Structure-Based Drug Design and Molecular Docking - Euro MedChem and CADD 2026 (France)
- Sustainable Biologics Manufacturing - Biologics Meet 2026 (UK)
- Synthetic and Green Medicinal Chemistry - Euro MedChem and CADD 2026 (France)
- Synthetic Biology & Bioengineering Approaches - Biotech-2026 (France)
- Target Identification and Validation - Euro MedChem and CADD 2026 (France)
- Targeted Oral and Gastro-Resistant Formulations - Drug Devilvery 2026 (France)
- Targeted Therapies in Cardiovascular Regeneration - Cardiovascular-2026 (France)
- Targeting the Renin-Angiotensin-Aldosterone System (RAAS) - Cardiovascular-2026 (France)
- The Role of CROs in Clinical Trial Execution - Clinical Trials-2026 (UK)
- Theranostics and Personalized Medicine - Drug Devilvery 2026 (France)
- Toxicology - Pharmacology 2026 (Italy)
- Toxicology & Safety Pharmacology - Euro Pharmacology 2026 (France)
- Track 01: Digital Marketing in Pharma Industry - Future Pharma 2026 (Netherlands)
- Track 02: The Future of Pharma R&D - Future Pharma 2026 (Netherlands)
- Track 03: Pharmaceutical Chemistry - Future Pharma 2026 (Netherlands)
- Track 04: Pharmaceutical Analysis - Future Pharma 2026 (Netherlands)
- Track 05: Pharmaceutics & Pharmacotherapeutics - Future Pharma 2026 (Netherlands)
- Track 06: Industrial Pharmacy and Physical pharmacy - Future Pharma 2026 (Netherlands)
- Track 07: Clinical and Hospital Pharmacy - Future Pharma 2026 (Netherlands)
- Track 08: Pharmaceutical and healthcare Industry - Future Pharma 2026 (Netherlands)
- Track 09: Regulatory Affairs and Intellectual Property Rights - Future Pharma 2026 (Netherlands)
- Track 10: Pharma and Biotech Financial Outlook - Future Pharma 2026 (Netherlands)
- Track 10: Pharmaceutical Engineering - Pharmaceuticalindustry-2025 (Netherlands)
- Track 11: Novel Drug Delivery Systems - Future Pharma 2026 (Netherlands)
- Track 11: Pharmaceutical Supply Chain Optimization - Pharmaceuticalindustry-2025 (Netherlands)
- Track 12: Drug Discovery and Development - Future Pharma 2026 (Netherlands)
- Track 12: Pharmaceutical Regulatory Requirements - Pharmaceuticalindustry-2025 (Netherlands)
- Track 13: Green and Community Pharmacy - Future Pharma 2026 (Netherlands)
- Track 13: Pharmaceutical Packaging Advances - Pharmaceuticalindustry-2025 (Netherlands)
- Track 14: Big data analytics and Pharma - Future Pharma 2026 (Netherlands)
- Track 1: Digital Parma - Pharmaceuticalindustry-2025 (Netherlands)
- Track 2: R&D Progress: The Path to New Medicines - Pharmaceuticalindustry-2025 (Netherlands)
- Track 3: Clinical Pharmacy and Therapeutics - Pharmaceuticalindustry-2025 (Netherlands)
- Track 4: Pharmaceutical sciences - Pharmaceuticalindustry-2025 (Netherlands)
- Track 5: Pharmaceutical Nanotechnology - Pharmaceuticalindustry-2025 (Netherlands)
- Track 6: Entrepreneurs Investment - Pharmaceuticalindustry-2025 (Netherlands)
- Track 7: The Globalized Pharmaceutical Industry - Pharmaceuticalindustry-2025 (Netherlands)
- Track 8: Drug Discovery - Pharmaceuticalindustry-2025 (Netherlands)
- Track 9: Drug Development - Pharmaceuticalindustry-2025 (Netherlands)
- Transdermal and Intradermal Delivery Systems - Drug-Delivery-2026 (France)
- Transdermal and Topical Drug Delivery - Drug Devilvery 2026 (France)
- Translational Research & Clinical Applications - Biotech-2026 (France)
- Types of Formulations - Formulations 2026 (UK)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
- Vaccine Delivery Technologies - Drug-Delivery-2026 (France)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2026 (UK)
- Vaccine Technologies & Immunotherapeutics - PHARMA BIOTECH 2026 (UK)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2026 (France)
- Veterinary & Comparative Pharmacology - Euro Pharmacology 2026 (France)
- Wearable and Implantable Drug Delivery Devices - Drug Devilvery 2026 (France)