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National Regulatory Process

Contribute to strengthening national regulatory authorities in selected countries of the hemisphere in pharmaceutical products and medical devices.


  • Conduct an annual Forum in 2012 and 2013 that builds upon the lessons learned and expressed outcomes of the 2011 Forum.
  • Produce and distribute materials that focus on additional themes pertaining to the Canadian regulatory process for biologics (including vaccines), pharmaceuticals and medical devices, throughout the pre- and post-market product lifecycle.


Última actualización el Jueves 21 de Febrero de 2013 12:51