Pharmacovigilance and Drug Safety
Pharmacovigilance and drug safety are essential elements of the pharmaceutical industry. In order to identify potential safety concerns and reduce risks, pharmacovigilance entails the systematic collection, analysis, and assessment of adverse drug reactions (ADRs). Pharmacovigilance assists in the detection of uncommon or chronic side effects that would not have been noticeable during clinical trials by regularly assessing the safety profile of medications. In addition to safeguarding patients, this proactive strategy improves the general caliber and effectiveness of therapeutic interventions. Novel developments in data analytics, real-time monitoring, and regulatory frameworks are always being made to guarantee drug safety and enhance the efficacy of pharmacovigilance systems.
- Adverse drug reactions monitoring
- Risk assessment and management
- Pharmacogenomics and personalized medicine
- Adverse drug reactions monitoring
- Risk assessment and management
- Pharmacogenomics and personalized medicine
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