000 01864nam  2200385zi 4500
0019.895027
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006m     o  d f      
007cr cn|||||||||
008210105t20212021onc     o    f000 0 eng d
020 |a9780660370422
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH164-310/2021E-PDF
24500|aIncident reporting for medical devices : |bguidance document.
264 1|aOttawa, ON : |bHealth Canada = Santé Canada, |c2021.
264 4|c©2021
300 |a1 online resource (iii, 15 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |a"January 2021."
500 |aCover title.
500 |a"Effective Date: June 23, 2021; supersedes: October 3, 2011."
500 |aIssued also in HTML format.
500 |aIssued also in French under title: Rapports d’incidents liés aux matériels médicaux : lignes directrices.
520 |a"The purpose of this guidance document is to assist manufacturers, importers and authorization holders in understanding and complying with the Medical Devices Regulations concerning incident reporting"--Introduction, page 1.
650 0|aMedical instruments and apparatus|xSafety regulations|zCanada.
650 0|aMedical instruments and apparatus|xGovernment policy|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tRapports d’incidents liés aux matériels médicaux : |w(CaOODSP)9.895029
85640|qPDF|s820 KB|uhttps://publications.gc.ca/collections/collection_2021/sc-hc/H164-310-2021-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/incident-reporting-medical-devices-guidance-2021.html