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Medical Devices Regulations ( SOR /98-282) - laws …
- https://laws-lois.justice.gc.ca/eng/regulations/SOR-98-282/
- Medical Devices Regulations. 1 - Interpretation; 2 - Application; 6 - Classification of Medical Devices; 8 - PART 1 - General. 8 - Application; 9 - Manufacturer’s Obligations; 10 - Safety and Effectiveness Requirements; 21 - …
Medical Devices Regulations ( SOR /98-282) - laws …
- https://laws-lois.justice.gc.ca/eng/regulations/SOR%2D98%2D282/FullText.html
Medical Devices Regulations ( SOR /98-282)
- https://laws.justice.gc.ca/eng/regulations/SOR-98-282/page-3.html
- 32.1 The Minister shall recognize a person as a registrar for the purpose of issuing, renewing, suspending or cancelling quality management system certificates if …
Legislation and Guidelines - Medical devices - Canada.ca
- https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/legislation-guidelines.html
- Acts and Regulations The Therapeutic Products Directorate (TPD) applies the Food and Drug Regulations and the Medical Devices Regulations under the authority of the …
Health Canada CMDR Updates 2021 – ComplianceAcuity
- https://www.complianceacuity.com/health-canada-cmdr-updates-2021/
- The SOR/98-282 changes that took effect on 23 June 2021 are expected to be incorporated into the Justice Laws website version within a couple weeks. The SOR/98-282 changes …
List of Acts and Regulations - Canada.ca
- https://www.canada.ca/en/health-canada/corporate/about-health-canada/legislation-guidelines/acts-regulations/list-acts-regulations.html
- This Act aims to protect the health of Canadians in light of conclusive evidence implicating tobacco use in the incidence of numerous debilitating and fatal …
MDSAP International Regulations [English] (Australia, …
- https://www.fda.gov/medical-devices/medical-device-single-audit-program-mdsap/mdsap-international-regulations-english-australia-brazil-canada-japan-and-usa
- Canada Medical Devices Regulations (SOR/98-282) Japan Japanese Medical Device QMS Requirements and other related Regulatory Information USA 21 CFR 803 …
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