ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements?

Added by Referral on 2019-03-13

Conference Dates:

Start Date Start Date: 2019-04-02
Last Date Last Day: 2019-04-02
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2019-03-31

Conference Contact Info:

Contact Person Contact Person: Ashutos Swain
Email Email: [email protected]
Address Address: 2479 E. Bayshore Road Suite 260, Palo Alto, CA, 94303, United States
Phone Fax: [email protected]

Conference Description:

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.
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