Post-Marketing Surveillance Insights
Post-marketing surveillance is now integral to understanding the long-term effects of medications once they are approved for public use. In addition to real-world data (RWD), advancements in data analytics and machine learning have allowed for more efficient analysis of large datasets to detect rare or delayed adverse drug reactions. This has led to faster response times in addressing safety concerns. Moreover, collaboration between regulatory bodies, healthcare providers, and pharmaceutical companies is strengthening pharmacovigilance efforts. Post-marketing surveillance also helps inform updates to drug labeling, provides insights into off-label uses, and supports better patient outcomes through ongoing monitoring and adjustments based on real-world use.
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- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Next Generation Approach of Antibiotics - Antibiotics Resistance 2025 (Canada)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Spain)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Transdermal and Intradermal Delivery Systems - Drug Delivery-2025 (Netherlands)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Trending: Digital Health and Telemedicine for Rare Care - ORPHAN DRUGS 2025 (France)
- Types of Formulations - Formulations 2025 (France)
- Vaccine Delivery Technologies - Drug Delivery-2025 (Netherlands)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Veterinary Pharmacology - Pharmacology-2025 (Spain)
- Women in Rare Disease Leadership and Science - ORPHAN DRUGS 2025 (France)