Attend this webinar to learn how to prepare and construct the technical file for medical device firms that meets the applicable regulatory requirements.

Date : 1st June 2017 to 1st June 2017

Place : United States, Fremont

Website :http://www.onlinecompliancepanel.com/webinar/EU-MEDICAL-DEVICE-REGULATIOIN-504418/JUNE-2017-ES-ALLCONFERENCEALERT

Contact Person:OCP Panel

Description:

Attend this webinar to learn how to prepare and construct the technical file for medical device firms that meets the applicable regulatory requirements.

Attend this webinar to learn how to prepare and construct the technical file for medical device firms that meets the applicable regulatory requirements. will be held in Fremont,United States on date 2017-06-01

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Deadline for abstracts/proposals : 31st May 2017

Keynote Speakers : David R. Dills, is an independent Global Regulatory Affairs & Compliance Consultant and has an accomplished record with more than 26 years of experience in regulatory affairs, compliance and quality consultative services for early-stage/established Class I/II/III medical devices, IVD's, and bio/pharmaceutical manufacturers on the global landscape. Previously employed, with increasing responsibilities by device manufacturers and consultancies, including a globally recognized CRO, has wor

Conference Highlights :This Webinar will provide a substantive overview and outlines how to prepare and construct the Technical File for those device firms dealing with the global regulatory landscape. The technical file is the key to a medical device's certification for CE marking because it contains the most important information about the device, how it works, how it is manufactured, and how it meets the applicable regulatory requirements. The Technical File is a comprehensive collection of information and doc

Venue :United States

Check the event website for more details.