Clinical Trials and Regulatory Affairs in Pharmacy
Clinical research work is directly associated to patient outcomes, such as in clinical trials. People within the clinical research field feel that their jobs are extremely impactful, as they are at the very forefront of wherever science becomes medicine that can improve patients' lives. Regulatory affairs (RA) scientists are involved overseeing the process of getting a drug or product through the FDA review and approval process and onto the market. Since every step in the process of product development is highly regulated, those in RA work at every step to move a drug from research and development through FDA approval.
- Products are developed
- Tested
- Marketed
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Clinical Trials and Regulatory Affairs in Pharmacy Conference Speakers
Recommended Sessions
- Advances in Pharmaceutical Packaging
- Clinical Trials and Regulatory Affairs in Pharmacy
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- Drug Discovery
- Drug Safety and Pharmacovigilance
- Peptides and Protein Drug Delivery
- Pharmacogenetics and Genomics
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- Drug Development
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- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Next Generation Approach of Antibiotics - Antibiotics Resistance 2025 (Canada)
- Toxicology - Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
- Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
- Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (France)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (France)