Overview

These module will provide insight into what the FDA is looking for during an audit and provide participants with tools and case studies for each of the topics.

Why Should You Attend

The FDA is a regulatory body that can shut down a manufacturing facility then the company loses time and money due to the closure. For this webinar series, we are providing the most common observations given by the FDA and provide ways to prevent these most common observations.

Webinar Takeaway

  • Who should be conducting an investigation?
  • When is an investigation necessary?
  • What constitutes an investigation?
  • What is a root cause?
  • What tools can be used to determine the root cause?
  • What if a root cause could not be determined?
  • Corrective Actions/Preventative Actions
  • Case Studies of Investigations and Actions

Case Study 1

Case Study 2

Case Study 3

Who will Benefit

  • Manufacturing Personnel (Associates and Supervisors) and Managers.
  • Quality Control Personnel (Associates and Supervisors)
  • Quality Assurance Personnel (Associates and Supervisors)
  • New Graduates just entering into the Pharmaceutical Manufacturing Industry

Industries who can attend

This 60-minute online course is intended for professionals in the Pharmaceutical, Clinical Data Management SaaS companies, and medical device companies . Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel

Faculty John E Lincoln


John E. Lincoln is Principal of J. E. Lincoln and Associates LLC, a consulting company, with over 32 years experience in U.S. FDA-regulated industries, 18 of which as a full time independent FDA-regulated industry consultant. Mr. Lincoln has worked with companies from start-up to Fortune 100, in the U.S., Mexico, Canada, France, Germany, Sweden, China and Taiwan. He specializes in quality assurance, regulatory affairs, QMS / CGMP audits and problem remediation and FDA responses, new / changed product 510(k)s, process / product / equipment including QMS and software validations, ISO 14971 product risk management files / reports, Design Control / Design History Files, Technical Files. He’s held positions in Manufacturing Engineering, QA, QAE, Regulatory Affairs, to the level of Director and VP (R&D).

Faculty John E Lincoln

Choose a Purchase Options

$289

Recorded Access Single - 6 month Access

You'll have access to one log-in for an archived recording of the entire 60-minute webinar, including the Q&A period, for 1 participant. You can log in any time of day or night. You'll also receive all presentation materials, plus an audio recording and transcript for the entire session. Delivery is approximately 48 hours after the session

$399

MP3 Download (DVD)

Within 48 hours delivered - Lifetime Access ,Audio recording of a webinar and reference manual delivered by download. Listen anytime on any compatible device.