2019 - Handling OOS Test Results and Completing Robust Investigations
Date2019-12-17
Deadline2019-12-17
VenueOnline Event, USA - United States
KeywordsOOS test results training; Implementing CAPA; OOS or atypical result
Topics/Call fo Papers
FDA requirements for handling OOS/ OOT results
Phase I- Laboratory Phase of Investigations
Phase II a Full Scale Investigation
Concluding an Investigation
Out-of Trend investigations
Common pitfalls during OOS Investigations
Review of recent OOS related citations in Warning Letters
Phase I- Laboratory Phase of Investigations
Phase II a Full Scale Investigation
Concluding an Investigation
Out-of Trend investigations
Common pitfalls during OOS Investigations
Review of recent OOS related citations in Warning Letters
Other CFPs
- Good Documentation Practice (GDocP) for FDA Regulated Industry
- Guidelines for Performing a Corporate Wide Internal Audit Risk Assessment
- Human Error Reduction Techniques for Floor Supervisors
- ISO 13485:2016 - What are the hot topics and changes?
- Hospital Utilization Management: From Foundation to New Trends
Last modified: 2019-11-05 17:26:46