Guidance document : regulatory enrolment process (REP) for medical devices.: H164-292/2024E-PDF
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publications.gc.ca/pub?id=9.882305&sl=0
| Department/Agency | Canada. Health Canada, issuing body. |
|---|---|
| Title | Guidance document : regulatory enrolment process (REP) for medical devices. |
| Variant title | Guidance document : regulatory enrolment process |
| Publication type | Monograph |
| Language | [English] |
| Other language editions | [French] |
| Format | Electronic |
| Electronic document | |
| Note(s) | Issued also in French under title: Ligne directrice : processus d'inscription réglementaire (PIR) pour les instruments médicaux. Title from cover. "Effective date: 2024/03/15." "Pub.: 230738"--Page 2. Includes bibliographical references. |
| Publishing information | [Ottawa] : Health Canada = Santé Canada, March 2024. ©2024 |
| Description | 1 online resource (22 pages) : illustrations |
| ISBN | 9780660699363 |
| Catalogue number |
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| Departmental catalogue number | 230738 |
| Subject terms | Medical instruments and apparatus -- Government policy -- Canada. Medical instruments and apparatus industry -- Government policy -- Canada. |
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