Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system.

Date : 26th October 2017 to 27th October 2017

Place : United States, San diego

Website :https://www.eventbrite.com/e/complaints-adverse-event-reporting-and-recalls-an-integrated-approach-ntz-tickets-32691256428?aff=NDT

Contact Person:Paula Edwards

Description:

Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system.

Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system. will be held in San diego,United States on date 2017-10-27

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Deadline for abstracts/proposals : 12th October 2017

Keynote Speakers : Dan O'Leary is President of Ombu Enterprises, LLC, a company offering training and execution in Operational Excellence, focused on analytic skills and a systems approach to operations management.

Conference Highlights :To have an effective and efficient QMS you need to understand how to implement the related QMS processes. Developing the processes involves implementing best practices

Venue :San Diego, CA 92101, United States

Check the event website for more details.