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:
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
Vancouver, Canada
June 02-03, 2025
31st International Conference on Advanced Clinical Research and Clinical Trials
Amsterdam, Netherlands
June 10-11, 2025
24th International Conference on Medicinal and Pharmaceutical Chemistry
Vancouver, Canada
June 10-11, 2025
7th International Conference and Exhibition on Pharmaceutical Development and Technology
Vancouver, Canada
June 16-17, 2025
18th International Conference and Exhibition on Pharmacovigilance & Drug Safety
Frankfurt, Germany
June 23-24, 2025
25th World Congress on Pharmaceutical Sciences and Innovations in Pharma Industry
Paris, France
September 08-09, 2025
26th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
Frankfurt, Germany
September 23-24, 2025
10th International Conference on Future Pharma and Innovations
Amsterdam, Netherlands
November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
Zurich, Switzerland
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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