Drug Regulatory Affairs
Regulatory Affairs is involved in the development of new medicinal products from early on, by integrating regulatory principles and by preparing and submitting the relevant regulatory dossiers to health authorities. Regulatory Affairs is involved in every step of the development of a novel medicine and in the post-marketing activities with medicinal products.
- Regulatory science
- Dosage form
- Thin-film drug delivery
Related Conference of Drug Regulatory Affairs
December 12-13, 2024
12th International Conference and Exhibition on Natural Products and Medicinal Plants Research
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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
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May 05-06, 2025
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June 10-11, 2025
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Drug Regulatory Affairs Conference Speakers
Recommended Sessions
- Biodrugs, Biomolecules and Therapeutics
- Biomaterials in Drug Delivery
- Biotherapy and Radiopharmaceuticals
- Blockchain-Pharmaceutical Advancements
- Challenges in Pharmaceutical Research
- Digital Therapeutics-Curative Therapies
- Drug Delivery Technologies
- Drug Design and Development
- Drug Discovery and Screening
- Drug Regulatory Affairs
- Drug Targeting and Drug Development
- Molecular Dynamics Simulations
- Novel Developments In Drug Delivery System
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- Pharmaceutical Formulations
- Pharmaceutical Microbiology and Biotechnology
- Pharmaceutical Nanotechnology
- Pharmaceutical Research & Development
- Pharmacogenetics
- Phenotypic Drug Discovery
- Precision Medicine
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