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| 02052cam 2200361zi 4500 |
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| 001 | 9.874301 |
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| 003 | CaOODSP |
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| 005 | 20221107164144 |
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| 006 | m o d f |
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| 007 | cr ||||||||||| |
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| 008 | 190723e201906##onc o f000 0 eng d |
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| 020 | |a9780660312163 |
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| 040 | |aCaOODSP|beng|erda|cCaOODSP |
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| 043 | |an-cn--- |
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| 086 | 1 |aH164-280/2019E-PDF |
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| 245 | 00|aMandatory reporting of serious adverse drug reactions and medical device incidents by hospitals : |bguidance document. |
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| 264 | 1|a[Ottawa] : |bHealth Canada = Santé Canada,|cJune 2019. |
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| 264 | 4|c©2019 |
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| 300 | |a1 online resource (iv, 40 pages) |
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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: Déclaration obligatoire des réactions indésirables graves à un médicament et des incidents liés aux instruments médicaux par les hôpitaux : document d’orientation. |
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| 500 | |aIssued also in HTML format. |
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| 520 | |a"The purpose of this guidance document is to provide hospitals with information that may be useful in achieving compliance with the federal regulatory requirement for hospitals to report serious ADRs and MDIs to Health Canada as outlined in section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical DeviceRegulations"--Objective, page 1. |
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| 692 | 07|2gccst|aHealth care facilities |
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| 692 | 07|2gccst|aSide effects |
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| 692 | 07|2gccst|aLegislation |
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| 710 | 1 |aCanada. |bHealth Canada. |
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| 775 | 08|tDéclaration obligatoire des réactions indésirables graves à un médicament et des incidents liés aux instruments médicaux par les hôpitaux : |w(CaOODSP)9.874303 |
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| 856 | 40|qPDF|s610 KB|uhttps://publications.gc.ca/collections/collection_2019/sc-hc/H164-280-2019-eng.pdf |
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| 856 | 4 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting/mandatory-hospital-reporting/drugs-devices.html |
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