Investigation and Root Cause Analysis to Meet FDA Expectations

Website https://www.compliance4all.com/control/w_product/~product_id=502546LIVE?channel=ourglocal_Jun_2019_S | Edit Freely

Category Educational webinars, Healthcare webinars, Biopharmaceutical, Laboratory Managers, pharmaceutical trainings

Deadline: June 24, 2019 | Date: June 26, 2019

Venue/Country: Online, U.S.A

Updated: 2019-04-22 16:20:08 (GMT+9)

Call For Papers - CFP

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

Email: compliance4all14gmail.com