Demystifying the Canadian Drug and Health Products Regulatory Landscape

Speaker

Instructor: Susanne Picard
Product ID: 706209
Training Level: Basic to Advanced

Location
  • Duration: 60 Min
This seminar will give you a snapshot of what is current, what is coming and what this means to anyone who is currently developing Drugs and other Health Products for the Canadian market. The focus will be on drugs, biologics and medical devices.
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Why Should You Attend:

In this seminar, we will demystify what the Canadian regulatory landscape is for efficient Canadian development initiatives; providing an overview of current Drug and Heath Product Regulatory Landscape and how it is currently evolving.

Areas Covered in the Webinar:

  • Current regulatory & submission requirements for drugs, biologics and medical devices as required by Canada’s Regulatory Agency, Health Canada.
  • Health Canada’s major reform and its impact on the regulatory environment.
  • Major initiatives and up-coming changes in the regulatory environment, including use of foreign reviews / decisions, international collaboration, improved access to different drugs, expansion of priority review pathways, the use of real-world evidence, the Medical Device Single Audit Program, and the digital health review division.
  • Best approaches for working with Health Canada in any drug and & health product development plan.

Who Will Benefit:

  • This seminar is for all regulatory or business development individuals or companies presently developing a drug or other health product who are considering the Canadian market, or the global North American market, including Canada.
Instructor Profile:

Susanne Picard
Founder and President, SPharm Inc

Founder and President of SPharm, Susanne Picard is a sought-after expert on all aspects of the regulatory landscape. SPharm is a leading regulatory affairs consultancy headquartered in Canada that services clients around the globe.

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