Best Practices for Conducting OOS Investigations (in Pharmaceutical Laboratories) 2013
11 Apr 2013
Webinar
Description
Topics
Phase I- Laboratory Phase of Investigations
FDA requirements for handling OOS/OOT results
Concluding an Investigation
Phase II – Full Scale Investigation
Common pitfalls during OOS Investigations
Out-of Trend investigations
Review of recent OOS related citations in Warning Letters
Who should Attend
QA personnel, QC Supervisors and Management, Documentation management specialists, QA Management and Regulatory affairs personnel.
Past Events
Best Practices for Conducting OOS Investigations (in Pharmaceutical Laboratories) 2013 - 11 Apr 2013, Webinar (14196)
Important
Please, check "Best Practices for Conducting OOS Investigations (in Pharmaceutical Laboratories)" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Hospitals & Clinics, Medical device, Medical laboratories, Pharma
