Loading Purplepass...
Tricks To Get The [Most Out] Of Your Device Master Records
Presented By Netzealous LLC DBA - Compliance4All
Wednesday, January 9th at 10:00am PST
Online sale ends: 01/08/19 at 11:30am PST
Online
161 Mission Falls Lane, Suite 216
Fremont, CA 94539
-= series =-
Buy Tickets
|
Talent
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: compliance4all14@gmail.com Additional Information
One Dial-in One Attendee
Price: $150.00
|
Presented By
10:00am to 11:30am
General Admission: $150.00
All Ages
50 18004479407 UPCOMING EVENTS
PAST EVENTS
Friday, November 16th
Online Past Event
|
