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| 01491nam 2200361zi 4500 |
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| 001 | 9.882305 |
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| 003 | CaOODSP |
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| 005 | 20240404152120 |
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| 006 | m o d f |
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| 007 | cr mn||||||||| |
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| 008 | 191121e202403 onca ob f000 0 eng d |
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| 020 | |a9780660699363 |
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| 040 | |aCaOODSP|beng|erda|cCaOODSP |
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| 043 | |an-cn--- |
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| 086 | 1 |aH164-292/2024E-PDF |
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| 245 | 00|aGuidance document : |bregulatory enrolment process (REP) for medical devices. |
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| 246 | 17|aGuidance document : |bregulatory enrolment process |
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| 264 | 1|a[Ottawa] : |bHealth Canada = Santé Canada, |cMarch 2024. |
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| 264 | 4|c©2024 |
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| 300 | |a1 online resource (22 pages) : |billustrations |
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| 336 | |atext|btxt|2rdacontent |
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| 337 | |acomputer|bc|2rdamedia |
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| 338 | |aonline resource|bcr|2rdacarrier |
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| 500 | |aIssued also in French under title: Ligne directrice : processus d'inscription réglementaire (PIR) pour les instruments médicaux. |
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| 500 | |aTitle from cover. |
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| 500 | |a"Effective date: 2024/03/15." |
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| 500 | |a"Pub.: 230738"--Page 2. |
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| 504 | |aIncludes bibliographical references. |
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| 650 | 0|aMedical instruments and apparatus|xGovernment policy|zCanada. |
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| 650 | 0|aMedical instruments and apparatus industry|xGovernment policy|zCanada. |
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| 710 | 1 |aCanada. |bHealth Canada, |eissuing body. |
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| 775 | 08|tLigne directrice : |w(CaOODSP)9.882308 |
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| 856 | 40|qPDF|s646 KB|uhttps://publications.gc.ca/collections/collection_2024/sc-hc/H164-292-2024-eng.pdf |
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