Labelling
All Medical Devices must be registered for sale in Canada and all labelling materials (package labels, cartons, and product inserts) must be compliant with Canadian Regulations and the marketing authorization for the product.
DSA offers pre-approval label reviews or label development to guide you on compliance with Canadian Regulations and advise you on changes to labelling which will help maximize claims and/or expedite product approvals.
DSA offers post-approval label reviews to ensure compliance with the marketing authorization or to help you determine if supplemental filings are required to support your proposed changes to the approved label.
Contact us today to find out how our Regulatory Team can be of assistance to you. For more information on services offered, click here to request a copy of our free brochure.
Make DSA Consultants Your Regulatory Compliance Strategic Partner Today
Call DSA Consultants today to discuss your unique professional needs.
(905) 827 - 0057
5006 South Service Road, Unit #6
Burlington, ON, L7L 5Y7
|
