ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements?
Website https://www.complianceonline.com/iso-14971-2012-medical-device-risk-analysis-ce-mark-requirements-we |
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Deadline: April 02, 2019 | Date: April 02, 2019
Venue/Country: U.S.A
Updated: 2019-02-11 16:17:00 (GMT+9)
Call For Papers - CFP
This webinar will benefit medical device companies planning to have a CE mark under the European Union Directive 93/42/EEC. We will discuss what is new in ISO 14971:2012 and help you avoid delays in obtaining or maintaining your CE mark for compliance to the Medical device Directive, EU Directive 93/42/EEC on Medical Devices.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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