Guidance Document - Private Label Medical Devices
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Medical Devices Guidance Documents, Health And Safety
Published
December 7, 2004
Last updated
March 15, 2011
Description
2005 (revised 2011) Health Canada document providing guidance on regulatory requirements for private label manufacturers of Class II, III and IV medical devices
Tags
Organization
Country / Region
Canada
License
Open Government License 2.0 (Canada)