Effective Records Management and Document Control for Medical Devices 2019 is a webinar that covers topics such as:
- Conducting Risk Assessment, Root Cause Analysis and Impact Assessment where appropriate
- Establishing best practice SOP, Deviation, CAPA, Change Controls, Complaint and Audit processes
- Improving efficiencies over the QMS tasks
- Creating Action Plans, and verifying their effectiveness
- Ensuring compliance to 21 CFR Part 11 and immutable audit trail
- Reducing the risks of manual error
- Taking the resource burden out of creating dashboards/ periodic reports
- Avoid observations, 483 letters and fines
Effective Records Management and Document Control for Medical Devices 2019 is intended for:
- Quality Assurance professionals
- Regulatory professionals
- Individuals involved with FDA compliance
- Executive Management
