Advancement Of Drug Regulatory Affairs

The term Regulatory  affairs  is a profession within regulated industries. Regulatory affairs have a very specific meaning within the healthcare companies. Regulatory affairs is a new profession which is  developed from the desire of governments to protect the  public health by controlling the efficacy and nature of the products in the fields such as 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 involved in every step of the development of a noval medicine and in the post-marketing activities with  medicinal products.

This track is representing  Regulatory & Pharmacovigilance  Regulatory compliance Regulatory requirements of pharmaceutical products  Marketing Authorizations Clinical Affairs & Regulatory Strategies Intellectual Property Rights

  • Clinical Trials & Pharmacovigilance
  • Regulatory compliance
  • Regulatory requirements of pharmaceutical products
  • Marketing Authorizations
  • Clinical Affairs & Regulatory Strategies
  • Intellectual Property Rights

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