Regulatory Affairs
Drug Regulatory Affairs refers to all aspects within the pharmaceutical development process and how they are subject to various degrees of regulation. The pharmaceutical law frame, guidelines covering Quality, Safety and Efficacy as well as Health Authorities' attitudes and requirements etc. have a great influence on the drug development process and the success of it. Regulatory affairs professionals deal with these aspects
Related Conference of Regulatory Affairs
February 27-28, 2025
8th International on Pharmacy and Pharmaceutical Conference
Prague, Czech Republic
April 07-08, 2025
4th International Conference and Expo on Pharmaceutics & Novel Drug Delivery Systems
Vancouver, Canada
May 05-06, 2025
17th International Conference on Pharmaceutical Education and Practice
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June 02-03, 2025
31st International Conference on Advanced Clinical Research and Clinical Trials
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June 10-11, 2025
24th International Conference on Medicinal and Pharmaceutical Chemistry
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7th International Conference and Exhibition on Pharmaceutical Development and Technology
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18th International Conference and Exhibition on Pharmacovigilance & Drug Safety
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June 23-24, 2025
25th World Congress on Pharmaceutical Sciences and Innovations in Pharma Industry
Paris, France
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26th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
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September 23-24, 2025
10th International Conference on Future Pharma and Innovations
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November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
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Regulatory Affairs Conference Speakers
Recommended Sessions
- Bio Pharmaceuticals
- Nano medicine and Biomedical Applications
- Pharmacognosy and Phytochemistry
- Pharmacology
- Regulatory Affairs
- Analytical and Bio analytical Techniques
- Clinical Pharmacy
- Drug Development
- Industrial Pharmacy
- Medicinal Chemistry
- Nanotechnology in Pharmaceuticals
- Pharmaceutical Manufacturing
- Pharmaceutical Microbiology
- Pharmaceutical Preformulation Studies
- Pharmaceutical sciences
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