Essentials of Complaint Handling and Medical Device Reporting 2017
15 Feb 2017
Webinar
Description
Topics
FDA Expectations, Regulations
Overview and Definitions
Processes and Procedures
Lessons Learned and Enforcement Case Studies
Investigating a complaint or MDR
Reportability Criteria
Common Mistakes and how to avoid them
Linkages between Complaint Handling, MDRs, and CAPA
Preparing for an FDA or NB Inspection
Best Practices
Who should Attend
Individuals participating in Failure Investigations
Complaint Specialists and Managers
Regulatory Affairs
Individuals analyzing returned products / Complaint Analysis
Clinical Affairs
Quality Engineers
Compliance Specialists
Complaint Handling Unit Personnel
Past Events
Essentials of Complaint Handling and Medical Device Reporting 2017 - 15 Feb 2017, Webinar (65335)
Important
Please, check "Essentials of Complaint Handling and Medical Device Reporting" official website for possible changes, before making any traveling arrangements
