Clinical Regulatory Affairs

Clinical Trials Are Heavily Regulated In Canada And Are Subject To The Internationally Recognized Set Of Regulations Referred To As Good Clinical Practices (GCPs)

With regulatory bodies like Health Canada being responsible for overseeing the regulatory compliance aspects for dietary supplements / natural health products, foods, medical devices, and cosmetics, and drugs, the regulatory landscape of clinical trials is broad and continuously evolving. As such, designing and executing a successful clinical trial benefits from partnering with a CRO with deep regulatory experience and a history of working with the regulatory bodies.

dicentra’s interdisciplinary team has unparalleled experience working with clients addressing all matters related to safety, quality, and compliance for all product categories in the life sciences and food industries.

Our team of clinical research professionals is ready to assist you in any or all phases of your clinical research project with an optimized and transparent approach to foster your research success.

  • 450+ clinical trials across our team
  • 200+ publications
  • 19 years in business
  • 1,200 clients globally

Contact us for assistance with regulatory affairs