Regulatory Affairs:
Regulatory affairs is a comparatively new profession which developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals , veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines. 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 actively involved in every stage of development of a new medicine and in the post-marketing activities with authorized medicinal products. The Regulatory Affairs department is an important part of the organizational structure of pharmaceutical industry. Internally it liaises at the interphase of drug development, manufacturing, marketing and clinical research. Externally it is the key interface between the company and the regulatory authorities.
- Importance and scope in pharma industry
- Regulatory procedure manual
- Regulatory Compliance
- Good Regulatory Practices
- Conflicts and Solution Trends in Regulatory issues
- Drug Design and development for compliancing with Regulatory Policies
- Code of Federal Regulations
Related Conference of Regulatory Affairs:
July 21-22, 2025
11th International Conference on Antimicrobials & Antibiotic Resistance
Vancouver, Canada
August 25-26, 2025
11th International Conference on Pharmaceutical Regulatory Affairs and IPR
Vancouver, Canada
September 08-09, 2025
26th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
Frankfurt, Germany
September 08-09, 2025
13th International Conference and Exhibition on Natural Products and Medicinal Plants Research
Frankfurt, Germany
September 15-16, 2025
42nd International Conference on Drug Discovery and Drug delivery system
Paris, France
September 22-23, 2025
20th International Conference on Pharmaceutical Formulations & Drug Delivery
Toronto, Canada
September 23-24, 2025
10th International Conference on Future Pharma and Innovations
Amsterdam, Netherlands
November 11-12, 2025
6th Annual Congress on Antibiotics and Bacterial Infections
Amsterdam, Netherlands
November 13-14, 2025
28th International Conference and Exhibition on Pharmaceutical Formulations
Paris, France
November 13-14, 2025
21st International Conference on Pharmaceutical Chemistry
Aix-en-Provence, France
November 25-26, 2025
4th World Congress on Medicinal Chemistry and Computer Aided Drug Design
Aix-en-Provence, France
November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
Zurich, Switzerland
January 28-29, 2026
23rd International Pharmaceutical Sciences & Life Saving Drugs
Bangkok, Thailand
Regulatory Affairs: Conference Speakers
Recommended Sessions
- Active Pharmaceutical Ingredients:
- Analytical strategies for pharmaceutical products:
- Biologics and Biosimilars :
- Clinical trials and Pharmacovigilance:
- Drug Delivery Technologies & Drug Designing and Development:
- Drug discovery and NCEs:
- Formulations and NNDS:
- Good Manufacturing Practices (GMP):
- Importance of Audit in Pharmaceutical Industry:
- Pharma Market Research:
- Pharmaceutical Auditing for OTC Drugs:
- Pharmaceutical Industry:
- Pharmaceutical Manufacturing, Scale Up and Tech transfer:
- Pharmaceutical Nanotechnology: Challenges and Opportunities:
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- Pharmaceutical Research and Development:
- Pharmacoeconomics:
- QC & QA: Quality control and Quality assurance:
- Quality by design(QbD) approach:
- Regulatory Affairs:
- Regulatory Authority Compliance:
- Use of Nanoparticles in DDS and Newer Methodologies:
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