Investigation and Root Cause Analysis to Meet FDA Expectations

MessageThis Webinar is over
Date Jun 26, 2019
Time 12:00 PM EDT
Cost $150.00
This live interactive presentation will also discuss the regulations associated with the detection, correction and prevention of human errors in GMP manufacturing and laboratory processes.

Why should you Attend:
We will focus on improved techniques to get to the real cause of the problem. With this information you will be able to develop meaningful CAPAs that have a chance to remedy these problems, the first time.

Areas Covered in the Session:
How to develop a true CAPA for these problems
Develop an efficient and effective CAPA system to remedy the ingrained problems
Identification and prevention of human error during data entry

Who Will Benefit:
Quality Assurance Personnel
Quality Control Personnel
Supply Chain and Logistics Managers
Regulatory Affairs Professionals

Speaker Profile:
Angela Bazigos is the CEO of Touchstone Technologies Inc. She has degrees in Microbiology and Computing and 40 years of experience in the Life Sciences, Healthcare & Public Health Services.

Event Fee: One Dial-in One Attendee Price: $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407


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