ISO 13485:2016 for Medical Device Manufacturers: Ensuring a Smooth Transition through Effective Preparation
August 31, 2017 - Toronto ON CA

Xtalks Life Science Webinars

ajuurinen@xtalks.com
Phone: 416 977 6555 x371
Fax: 416 977 6999

This webinar will highlight best practices, suggestions and other information, including: - Understanding when medical device manufacturers will be required to comply with ISO 13485, and if there are any exceptions - Learning about the top ten changes that should be considered when identifying a compliance strategy - Discovering approaches that medical device manufacturers can utilize to effectively address the new standard

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