Difference between revisions of "File:FRM-0090 Authorization for medical devices mandatory problem foreign risk notification and recall reporting EN v22.docx"
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(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)
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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
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| 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 |
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