Guidance document : preparation of premarket medical device licence and licence amendment application for dermal fillers / published by authority of the Minister of Health.: H13-9/2-2017E-PDF

"Guidance documents are meant to provide assistance to industry and health care professionals on how to comply with governing statutes and regulations. They also serve to provide review and compliance guidance to staff, thereby ensuring that mandates are implemented in a fair, consistent and effective manner. ... This guidance document is intended to aid manufacturers and regulatory representatives in preparing medical device licence applications for dermal fillers"--p. i and p. 3.

Permanent link to this Catalogue record:
publications.gc.ca/pub?id=9.849009&sl=0

Publication information
Department/Agency Canada. Health Canada.
Collaborating author Canada. Health Products and Food Branch.
Title Guidance document : preparation of premarket medical device licence and licence amendment application for dermal fillers / published by authority of the Minister of Health.
Variant title Preparation of premarket medical device licence and licence amendment application for dermal fillers
Publication type Series - Browse issue records
Language [English]
Other language editions [French]
Format Electronic
Electronic document
Note(s) Cover title.
"Date adopted: 2016/11/24. Effective date: 2017/01/16".
Issued by Health Products and Food Branch.
Issued also in French under title: Préparation de demandes d’homologation et de modification d’homologation de matériels médicaux pour les produits de remplissage cutané.
Publishing information [Ottawa] : Health Canada, c2017.
Description 17 p.
Catalogue number
  • H13-9/2-2017E-PDF
Subject terms Regulation
Health protection
Personal care products
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