Difference between revisions of "File:FRM-0090 Authorization for medical devices mandatory problem foreign risk notification and recall reporting EN v22.docx"
Jump to navigation
Jump to search
(Authorization for medical devices mandatory problem, foreign risk notification, and recall reporting according to sections 61.1, 61.3 and 65.1 of the Medical Devices Regulations and/or designation to Act as the Canadian regulatory contact) |
(No difference)
|
Latest revision as of 12:09, 9 June 2021
Summary
Authorization for medical devices mandatory problem, foreign risk notification, and recall reporting according to sections 61.1, 61.3 and 65.1 of the Medical Devices Regulations and/or designation to Act as the Canadian regulatory contact
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Dimensions | User | Comment | |
---|---|---|---|---|
current | 12:09, 9 June 2021 | (111 KB) | Hc.mdd.postmarket-postcommercialisation.dim.sc (talk | contribs) | Authorization for medical devices mandatory problem, foreign risk notification, and recall reporting according to sections 61.1, 61.3 and 65.1 of the Medical Devices Regulations and/or designation to Act as the Canadian regulatory contact |
You cannot overwrite this file.
File usage
The following page uses this file: