Investigation and Root Cause Analysis to Meet FDA Expectations

Event Details

  • DateTue 06 August 2019
  • Time10:00 AM - 11:00 AM
  • VenueOnline
  • Location161 Mission Falls Lane, Suite 216, Fremont National 9453
  • TypeWorkshop
  • Ticket$$150 per person
  • Table$Price for a table per table (seats Normally between 8-12)
  • ContactNetzealous LLC DBA - Compliance4all
    8004479407
Register for this event

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: compliance4all14@gmail.com