Health Canada recently revised its GD210 document, which provides guidance to CMDCAS-recognized registrars on how to perform audits to ISO 13485:2003. Find out which additions and changes will have an impact on your next audit by downloading this recording of Intertek's webinar. The speaker, Intertek medical program manager Christine Forcier, will use her extensive background and expertise in the CMDCAS program to guide you through the changes, including: 

• How an applicable Medical Devices Regulations (MDR) requirement can be incorporated in to your quality management system (QMS) documentation 
• What information your registrar needs to gather prior to each on-site audit 
• How virtual manufacturers and regulatory correspondents shall be included in the audit
• Information on the License Amendment and Obligation To Inform

This valuable webinar will help you understand your registrar's expectations BEFORE your next audit. Download your copy today by completing the form below. Fields marked with a red asterisk (*) are required.