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:
November 25-26, 2025
4th World Congress on Medicinal Chemistry and Computer Aided Drug Design
Paris, France
November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
Zurich, Switzerland
December 15-16, 2025
3rd International Conference on Current Advances In Pharmaceutical Industry And development
Amsterdam, Netherlands
January 28-29, 2026
23rd International Pharmaceutical Sciences & Life Saving Drugs
Bangkok, Thailand
March 24-25, 2026
11th International Conference on Future Pharma and Innovations
Amsterdam, Netherlands
June 08-09, 2026
8th International Conference and Exhibition on Pharmaceutical Development and Technology
San Diego, USA
June 08-09, 2026
25th International Conference on Medicinal and Pharmaceutical Chemistry
San Diego, USA
July 27-28, 2026
26th World Congress on Pharmaceutical Sciences and Innovations in Pharma Industry
Rome, Italy
July 27-28, 2026
19th International Conference and Exhibition on Pharmacovigilance & Drug Safety
Rome, Italy
August 20-21, 2026
32nd International Conference on Advanced Clinical Research and Clinical Trials
London, UK
November 19-20, 2026
14th International Conference and Exhibition on Natural Products and Medicinal Plants Research
Dubai, UAE
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:
- Pharmaceutical Packaging and Logistics:
- 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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