Organization Name / Organize By
complianceonline
Organizing/Related Departments
Sales & marketing
Organization Type
Event Organizing Company
WebinarCategory
Technical
WebinarLevel
All (State/Province/Region, National & International)
Related Industries
Manufacturing
Medical/Healthcare/Hospital
Location
San Jose, California, United States
Attendees will learn how to streamline and conduct timely OOS and OOT investigations that meet FDA GMP expectations.
- Responsibility of the Analyst
- Responsibility of the Supervisor
- Obvious error
- Retesting
- Resampling
- Result validation
- Initiation of a production investigation.
- Invalidation of the initial result and accept the retest result.
Address/Venue
Online Event, 6201 America Center Drive
Suite 240
San Jose, CA 95002, USA