Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing Organizations
This guidance document provides medical device stakeholders with information on the requirements that the Therapeutics Products Directorate will use in recognizing Auditing Organizations under the MDSAP.
- Publisher
- Health Canada
- Resources
- 2
- Catalogue metadata updated
- 2023-12-02
Data overview
- Formats
- HTML
- File languages
- English, French
Official sources and licences
Resources
- Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing Organizations (English, HTML) HTML
- Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing Organizations (French, HTML) HTML