ISO 13485:2016 - What are the hot topics and changes?
Website https://www.complianceonline.com/iso-13485-2016-hot-topics-and-changes-webinar-training-705864-prdw? |
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Deadline: January 28, 2019 | Date: January 28, 2019
Venue/Country: U.S.A
Updated: 2018-12-30 04:02:53 (GMT+9)
Call For Papers - CFP
The ISO 13485:2016 is the essential standard for quality management systems for medical device manufacturer, importer, distributors and dealers in Europe and in the international markets. This standard has received some changes e.g. responsibility of outsourced processes, computer system validation, control of nonforming products etc. The understanding of this changes and how to implement last minute changes until March 2019 is essential to keep the certificates valid after March 2019.Introduction and who should apply the ISO 13485:2016Overview about the changes of the ISO 13485:2016Explaining of each changeSmart and fast ways to implement the changes in your quality management systemFast track internal audit to approve the changesAttend this webinar to understand, what are the changes to the previous standard and how to implement the changes in your current quality management system in a simple and quick way. Your implementation time until March 2019 is short and need smart ideas to reach the right level to pass the quality management audit by your certification company.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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