Effective Records Management and Document Control for Medical Devices
Website https://www.complianceonline.com/effective-records-management-and-document-control-for-medical-devic |
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Deadline: May 07, 2019 | Date: May 07, 2019
Venue/Country: U.S.A
Updated: 2019-04-05 16:45:34 (GMT+9)
Call For Papers - CFP
In this webinar attendees will learn the QSR and ISO 13485 requirements for document control and the ideas associated with the development and control of quality documentation. Also attendees will get knowledge on methods and practices that will improve the clarity and control of your document control system. Effective GMP documentation practices will be reviewed to ensure your paperwork is clear, complete, and easy to understand.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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