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Oct 23, 2024 · Regulatory modernization initiatives enhance economic growth by creating a more attractive business environment and encourage innovation by promoting partnership between regulators and Canadians to support new ideas and approaches for improving regulations.
- What We Heard: Report on Regulatory Modernization - Canada
In summer 2019, the Treasury Board of Canada Secretariat...
- Consultation summary: Clinical trials regulatory ... - Canada
Key aspects of the clinical trial regulatory modernization...
- What We Heard: Report on Regulatory Modernization - Canada
In summer 2019, the Treasury Board of Canada Secretariat (TBS) launched consultations on the following four regulatory modernization initiatives through the Canada Gazette: targeted Regulatory Reviews (round 2) review of the Red Tape Reduction Act. options to legislate changes to regulator mandates.
Key aspects of the clinical trial regulatory modernization initiative include: Agile life cycle: introduces a single authorization for trials involving multiple product types. It also offers greater agility in the oversight of clinical trials over their life cycle.
Jun 19, 2024 · Bill S-6. An Act respecting regulatory modernization. Status. In committee (House), as of June 19, 2024. Subscribe to a feed (what's a feed?) of speeches and votes in the House related to Bill S-6. Summary. This is from the published bill. The Library of Parliament often publishes better independent summaries.
Health Canada Regulatory Modernization: Yesterday, Today, And Tomorrow. Overview. itiative on improving regulatory review of drugs and devices (R2D2)1 . The goal of this initiative was to develop an agile regulatory system that supports.
Apr 5, 2022 · This enactment amends various Acts as part of the Regulatory Modernization Initiative in order to repeal or amend provisions that have, over time, become barriers to innovation and economic growth or to add certain provisions with a view to support innovation and economic growth.
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May 20, 2021 · On May 20, 2021 Health Canada opened a consultation on its proposal to modernize the regulatory framework for clinical trials related to human drugs, medical devices, non-prescription drugs, and natural health products to seek feedback from key stakeholders to validate and inform further policy development.
