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Pharmaceutical Regulatory Affairs in Latin America (London, United Kingdom - November 27-29, 2017) - Research and Markets
[September 27, 2017]

Pharmaceutical Regulatory Affairs in Latin America (London, United Kingdom - November 27-29, 2017) - Research and Markets


The "Pharmaceutical Regulatory Affairs in Latin America" conference has been added to Research and Markets' offering.

This comprehensive three day seminar will provide a detailed overview of how to gain a successful Marketing Authorisation in Latin America.

The course will provide you with:

  • An up-to-date coverage of the requirements that underpin successful Marketing Authorisation applications for pharmaceutical products across Latin America
  • The official regulatory information
  • Interpretation and alternatives to local and specific legal requirements
  • Hands-on experience in the region
  • An overview of the regulatory aspects of site inspections
  • Requirements for the marketing of NCE, biologic and biotechnology products, generic drugs and OTC medicines

Regulatry requirements for the Pharmaceutical Markets across Latin America including Columbia, Peru, Brazil, Mexico, Argentina, Uruguay, Paraguay, Venezuela, Ecuador, Central America, Chile

This seminar can be viewed both as an Introductory and a Refresher course and will provide you with:-

  • An up-to date coverage of the requirements that underpin successful marketing authorisation applications for pharmaceutical products across Latin America
  • The official regulatory information
  • Interpretation and alternatives to local and specific legal requirements
  • Hands-on experience in the region
  • An overview of the regulatory aspects of site inspections
  • Requirements for the marketing of NCE, Biologic and biotechnology products, generic drugs and OTC medicines

The following topics will be covered during the 3 days


  • Latin American demographics and market characteristics
  • Current legislation for key LA countries
  • Product Marketing Authorisation Requirements
  • Marketing Authorisation Modifications
  • Stability Requirements
  • Packaging and Labelling
  • Advertising regulations
  • Bioequivalence
  • Biologic and biotechnology product regulations

For more information about this conference visit https://www.researchandmarkets.com/research/nf4zx6/pharmaceutical


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