FDA Inspection’s 2020 - 7 secrets about Managing Your FDA Inspection’s 483 Observations Webinar
Topics/Call fo Papers
FDA’s is authorized to inspect regulated facilities and point out problems. How a firm responds to the inspection and how it plans to correct the problems has a significant impact on how FDA treats the firm after an inspection.
FDA inspections look for noncompliance with applicable manufacturing regulations. During the inspection the FDA investigator makes a “list of observations” that gives examples of violations.
Inspection procedure for identifying noncompliant practices
Discussions during the inspection with the FDA
Speaker:
Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He conducted domestic and foreign inspections
FDA inspections look for noncompliance with applicable manufacturing regulations. During the inspection the FDA investigator makes a “list of observations” that gives examples of violations.
Inspection procedure for identifying noncompliant practices
Discussions during the inspection with the FDA
Speaker:
Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He conducted domestic and foreign inspections
Other CFPs
- Best Practices To Help You Pass An FDA Computer System Validation Audit Training
- 10 Facts about Detailed Investigations: How to avoid an observation - Webinar
- 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
- 2021 International Conference on Computer, Blockchain and Financial Development
Last modified: 2020-11-27 00:08:54