File:FRM-0090 Authorization for medical devices mandatory problem foreign risk notification and recall reporting EN v22.docx
Revision as of 12:09, 9 June 2021 by 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)
FRM-0090_Authorization_for_medical_devices_mandatory_problem_foreign_risk_notification_and_recall_reporting_EN_v22.docx (file size: 111 KB, MIME type: application/vnd.openxmlformats-officedocument.wordprocessingml.document)
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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
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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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