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020 |a9780660797571
040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH164-414/2025E-PDF
24500|aTable of contents post-market submission guidance.
264 1|aOttawa, ON : |bHealth Canada = Santé Canada, |cNovember 2025.
264 4|c©2025
300 |a1 online resource (8 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aCover title.
500 |aIssued also in French under title: Lignes directrices sur les présentations après la mise en marché pour les table des matières.
520 |a"Not all folders (headings) are required for every submission. While the Table of Contents (ToC) is used for these interactions, only select folders are required for post-market submissions, and content guidance is specific to this context"--Heading classifications and content examples, page 3.
650 0|aMedical instruments and apparatus|xGovernment policy|zCanada.
650 0|aMedical instruments and apparatus|xLabeling|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tLignes directrices sur les présentations après la mise en marché pour les table des matières.|w(CaOODSP)9.957381
85640|qPDF|s503 KB|uhttps://publications.gc.ca/collections/collection_2026/sc-hc/H164-414-2025-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/international-medical-device-regulators-forum/post-market-submission.html
986 |a250345