Clinical Trials & Safety Monitoring
Clinical trials and pharmacovigilance are increasingly interconnected, with real-time safety monitoring playing a central role in assessing the long-term effects of new treatments. Recent research has emphasized the integration of real-world data (RWD) and AI-driven analytics to detect adverse drug reactions (ADRs) earlier. By linking clinical trial data with pharmacovigilance databases, researchers can improve post-marketing surveillance and ensure continued drug safety after approval. These advancements are crucial for rapidly identifying emerging safety concerns, enhancing patient protection, and ensuring that newly approved drugs maintain their therapeutic benefit across diverse populations.
Related Conference of Clinical Trials & Safety Monitoring
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&
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Clinical Trials & Safety Monitoring Conference Speakers
Recommended Sessions
- Adaptive Trial Models in Research
- Advancements in Pharmacovigilance
- Advances in Drug Discovery
- Biomarker Discovery in Drug Development
- Cancer Clinical Research Progress
- Clinical Data & Analytics Strategies
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- Clinical Trial Auditing Innovations
- Clinical Trial Efficiency Factors
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- Clinical Trials & Safety Monitoring
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- Decentralized Trial Models
- Drug Delivery & Blood-Brain Barrier
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