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

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April 14-15, 2025

18th European Biosimilars Congress

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19th World Drug Delivery Summit

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3rd Global Online Summit on Nanoscience and Nanotechnology

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38th World Congress on Pharmacology

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40th World Congress on Pharmacology and Therapeutics

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Pharma Biotech Expo

Toronto, Canada
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10th International Conference on Future Pharma and Innovations

Amsterdam, Netherlands
November 27-28, 2025

4th World Congress on Precision and Personalized Medicine

Zurich, Switzerland
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4th World Conference on Pharma Industry and Medical Devices

Zurich, Switzerland
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13th International Conference on Clinical Trials

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Regulatory Affairs: Conference Speakers

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