Netzealous LLC DBA - Compliance4All, Online
2019-01-09
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
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
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