Regulatory Affairs and Drug Approval
Regulatory Affairs and Drug Approval focuses on the processes and policies governing the development, evaluation, and authorization of pharmaceuticals. This track will explore global regulatory frameworks, submission requirements, and approval pathways across major agencies like FDA, EMA, and others. Topics include compliance, clinical trial regulations, documentation standards, and post-marketing surveillance. Emphasis will be placed on aligning scientific innovation with regulatory expectations to ensure the timely delivery of safe, effective, and high-quality medicines to patients.
Related Conference of Regulatory Affairs and Drug Approval
June 23-24, 2025
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Regulatory Affairs and Drug Approval Conference Speakers
Recommended Sessions
- Biologics and Biosimilars
- Cardiovascular and Renal Pharmacology
- Clinical and Translational Pharmacology
- Clinical Trials and Real-World Evidence
- Drug Discovery and Development
- Emerging Therapeutic Modalities
- Ethnopharmacology
- Immunopharmacology and Inflammation
- Molecular and Cellular Pharmacology
- Natural Product Pharmacology
- Neuropharmacology and Psychopharmacology
- Pediatric and Geriatric Pharmacology
- Pharmaceutical Nanotechnology
- Pharmacogenomics and Precision Medicine
- Pharmacokinetics and Pharmacodynamics
- Pharmacology in Public Health
- Pharmacovigilance and Drug Safety
- Regulatory Affairs and Drug Approval
- Toxicology and Safety Pharmacology
- Veterinary Pharmacology
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