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020 |a9780660449586
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH164-343/2022E-PDF
24500|aGuidance on releasing information from adverse reaction and medical device incident reports to the public.
264 1|aOttawa, ON : |bHealth Canada = Santé Canada, |cAugust 2022.
264 4|c©2022
300 |a1 online resource (iii, 12 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aIssued also in French under title: Lignes directrices sur la divulgation au public de renseignements tirés des déclarations d'effets indésirables et d'incidents liés aux instruments médicaux.
500 |aIssued also in HTML format.
650 0|aHealth products|xGovernment policy|zCanada.
650 0|aDrugs|xSide effects|xReporting|xGovernment policy|zCanada.
650 0|aMedical instruments and apparatus|xGovernment policy|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tLignes directrices sur la divulgation au public de renseignements tirés des déclarations d’effets indésirables et d’incidents liés aux instruments médicaux.|w(CaOODSP)9.914274
85640|qPDF|s993 KB|uhttps://publications.gc.ca/collections/collection_2022/sc-hc/H164-343-2022-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/guidance-adverse-reaction-medical-device-incident-reports.html