2019 - Powerful Closed-loop CAPA - Meeting FDA Expectations
Date2019-11-06
Deadline2019-11-06
VenueOnline Event, USA - United States
KeywordsFDA Compliant CAPA; GMP Audit; Non-conformance
Topics/Call fo Papers
U.S. FDA's CAPA Expectations
What is Closed-loop CAPA?
Correction, Corrective Action, Preventive Action
Failure Investigation Using an FI Template
7 Powerful Tools for Root Cause Analysis
Investigation Detail - Root or Probable Cause
Impact - Often Neglected but of Major Importance
Effectiveness - Determining and Monitoring
Institutionalize vs. Entropy
What is Closed-loop CAPA?
Correction, Corrective Action, Preventive Action
Failure Investigation Using an FI Template
7 Powerful Tools for Root Cause Analysis
Investigation Detail - Root or Probable Cause
Impact - Often Neglected but of Major Importance
Effectiveness - Determining and Monitoring
Institutionalize vs. Entropy
Other CFPs
- US FDA Medical Device QSR, 21 CFR 820 and Quality Management System
- Fair Debt Collection Practices Act - FDCPA, FCRA, Easily-Broken HIPAA, Civil Liability, Bad Check Laws, Promissory Notes, Mini-Miranda Warning
- HIPAA Audits and Enforcement for 2020 and Beyond - Current Issues and Focus for HIPAA Compliance in the Coming Year
- Female to Female Hostility @Workplace: All you need to Know
- EU ISO 13485:2016 Medical Device Quality Management System
Last modified: 2019-07-06 21:19:04