000 01563cam  2200349zi 4500
0019.867727
003CaOODSP
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006m     o  d f      
007cr |||||||||||
008190129t20192019onc    |o    f00| 0 eng d
020 |a9780660294247
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH164-268/2019E-PDF
24500|aGuidance document : |bmanagement of applications for medical device licenses.
264 1|a[Ottawa] : |bHealth Canada = Santé Canada, |c2019.
264 4|c©2019
300 |a1 online resource (22 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aIssued also in French under title: Ligne directrice : gestion des demandes d'homologation d'instruments médicaux.
500 |aCover title.
500 |aIssued also in HTML format.
500 |a"Date adopted: 2001/03/27. Date posted: 2019/11/08. Effective date: 2020/04/01."
650 0|aMedical instruments and apparatus industry|xLicenses|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tLigne directrice : |w(CaOODSP)9.867729
85640|qPDF|s291 KB|uhttps://publications.gc.ca/collections/collection_2020/sc-hc/H164-268-2019-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/policies/management-applications-medical-device-licences-investigational-authorizations/guidance-document.html