Tricks To Get The [Most Out] Of Your Device Master Records

Date : 9th January 2019 to 9th January 2019

Place : United States, Fremont

Website :https://www.compliance4all.com/control/w_product/~product_id=502267LIVE?channel=allconferencealerts_Jan_2019_SEO

Contact Person:Event Manager

Description:

Overview: It will also consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, as well as the two different device classification schemes. Required and desirable contents will be discussed. Why should you Attend: One of our most popular webinars, continuously updated with the latest U.S. FDA and European Union requirements. As U.S. companies go global, they must meet different product design documentation. Areas Covered in the Session: DHF "Typical" Contents and Deliverables The DMR and DHR / Lot / Batch Record TF / DD Required Contents Parallel Approaches to Documentation - Teams FDA and NB Audit Focus Who Will Benefit: QA RA R&D Engineering Production Operations Marketing Speaker Profile: John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. Event Fee: One Dial-in One Attendee Price: US $150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: [email protected]

Tricks To Get The [Most Out] Of Your Device Master Records will be held in Fremont,United States on date 2019-01-09

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Deadline for abstracts/proposals : 8th January 2019

Keynote Speakers :

Venue :Fremont, CA, USA

Check the event website for more details.