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

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Category Engineering, Production, Operations, Marketing

Deadline: January 07, 2019 | Date: January 09, 2019

Venue/Country: Online, U.S.A

Updated: 2018-11-07 15:07:08 (GMT+9)

Call For Papers - CFP

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: compliance4all14gmail.com