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March 09
webinar
Mar 9, 2018
Credits:

Overview: An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Why should you Attend: Observations that test methods are inadequate or the firm does not have appropriate data that demonstrates the method performs as intended rank high on the list of observations in the laboratory. Areas Covered in the Session: FDA System Based Inspection Guidance Laboratory Control System Most common observations in the laboratory Warning letter observations and analysis Who Will Benefit: Quality Control Manager Supervisors Analysis and Microbiologists Speaker Profile: John (Jerry) Lanese is an independent consultant with a focus on Laboratory Controls, Quality Systems and the components of an effective Quality System as they apply to the pharmaceutical and medical device industries and their suppliers to those industries. He received a BA and MS from Middlebury College and a Ph.D. in Analytical Chemistry from the University of Michigan. Event Fee: One Dial-in One Attendee Price: US$150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com

Member Price: 150.00 Non Member Price:

Contact Information

Event Manager Netzealous LLC DBA - Compliance4All 161 Mission Falls Lane, Suite 216, Fremont, CA 94539 United States of America 18004479407 (Tel) 302-288-6884 (Fax) support@compliance4All.com