Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies – Webinar By ComplianceOnline
| July 25, 2012 |
Online Event
This FDA Inspection training provides concrete strategies for planning remediation projects.
Why Should You Attend:
Today’s manufacturing and quality environments are highly automated and computerized. Manufacturers facing FDA pre-approval inspections (PAI) as well as those who will be re-inspected following inspectional observations (FDA-483), warning letters and other compliance issues can expect FDA to pay increasing attention to automated manufacturing systems and computerized quality systems. Read more »