Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements in a Cost Effective Manner - Webinar By GlobalCompliancePanel

6 October 2011, Wilmington, United States


Introduction
This webinar will provide valuable assistance to all regulated companies, since a CAPA program is a requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields.
Venue
online training webinar

online training webinar, 1000 N West Street, de, Suite 1200, Wilmington, 19801, United States

Organised by
global compliance panel
Contact information
Mr webinar web
online training webinar, Suite 1200, 1000 N West Street, Wilmington, 19801, United States of America
18004479407
Contact us by email

Search
 
 
Showing all upcoming events
Start Date
End Date
Location
Subject area
Event type

Advertisement
Spotlight


E-mail Enquiry
*
*
*
*