Medical Device 2012 - Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction
Date2012-02-20
Deadline2012-02-20
VenuePalo Alto, USA - United States
KeywordsISO 14971 Risk Reduction; Root Causes Analysis; Advanced Methods of RCA; FDA requirements for RCA; FDA QS requirements; FMEA; Root Causes Analysis Methods; Risk Analysis; Risk Reduction
Topics/Call fo Papers
This 90-minute webinar on Advanced Methods of Root Causes Analysis, for medical device companies, will cover principles and methods of Root Cause Analysis (RCA) and review proven techniques for ISO 14971 Risk Reduction based on RCA.
Why Should You Attend:
Root Cause Analysis (RCA) is the most important tool in device recall investigations and for preventing the adverse events. Unfortunately there is substantial misunderstanding of the limitations of the tool and how to use it correctly. The result is often wrong judgments, wrong design changes, and wasted efforts. Doing it right will reduce costs. Using advanced methods will make a big difference in preventing recalls.
Other CFPs
- Complaint Handling in Compliance with FDA and ISO Regulations
- Medical Device Regulations and Law in the US, EU and Canada
- Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment
- Software Verification and Validation Planning and Implementation
- CRO or ARO: How to Hire and Manage One
Last modified: 2012-01-23 15:15:07