FDA 483 Observations in the Laboratory. What went wrong? How can they be avoided? - Webinar By GlobalCompliancePanel

10 January 2012, Wilmington, United States


Introduction
In order to proactively address areas of concern to the FDA and other regulators, All units within each pharmaceutical firm should review recent regulatory observations and proactively establish programs or systems to address the regulatory concerns.
Venue
online training

online training, DE, 1000 N West Street, Wilmington, 19801, United States

Organised by
GlobalCompliancePanel
Contact information
Mr webinars web
Online Training, 1000 N West Street Suite,, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email

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

Advertisement
Spotlight


E-mail Enquiry
*
*
*
*