Investigation and Root Cause Analysis to Meet FDA Expectations

Date : 6th August 2019 to 6th August 2019

Place : United States, Fremont

Website :https://www.compliance4all.com/control/w_product/~product_id=502521LIVE?channel=allconferencealerts_Aug_2019_SEO

Contact Person:Event Manager

Description:

Overview: This webinar will help you understand the critical ingredients for conducting an effective root cause analysis, also you will learn how to Analyze and document the root cause of the problem. Why should you Attend: The billions of dollars spent by industry annually on quality / GMP are not providing the product safety or efficacy seemingly promised. Areas Covered in the Session: Use the 7 Tools to Find the Solution(s) Monitor for Effectiveness Lock In the Change - Close the Loop Take It to the Next Level Who Will Benefit: R&D Engineering Production Operations Speaker Profile: John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. Event Fee: One Dial-in One Attendee Price: US $150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: [email protected]

Investigation and Root Cause Analysis to Meet FDA Expectations will be held in Fremont,United States on date 2019-08-06

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Deadline for abstracts/proposals : 5th August 2019

Keynote Speakers :

Venue :Fremont, CA, USA

Check the event website for more details.