Detailed Investigations 2020 - 10 Facts about Detailed Investigations: How to avoid an observation - Webinar
Topics/Call fo Papers
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.
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
Who should be conducting an investigation?
When is an investigation necessary?
Speaker:
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.
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
Who should be conducting an investigation?
When is an investigation necessary?
Speaker:
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.
Other CFPs
- Live Webinar How to Implement a Compliant Training Program and Reduce Human Error
- FDA’s Technology Modernization Action Plan (TMAP) and Impact on Regulated Computer Systems and Data
- 7th International Conference on Data Mining (DaMi 2021)
- Remotely On boarding Your New Hire: Policies Practices and Processes
- Equal Employment Opportunity Compliance for Supervisors
Last modified: 2020-11-30 21:54:27