Implementing Management Responsibility for Medical Devices is a webinar that covers topics such as:
- Subject Areas covered
- Valuable documents that provide understanding
- QSR Preamble
- Quality System Regulation (QSR), including the definitions
- FDA`s Quality System Inspection Technique (QSIT) manual
- ISO 13485:2003
- Warning Letters
- Organization
- Quality policy
- Resources
- Responsibility and authority
- Management review
- Management Representative
- Quality system procedures
- Quality planning
Implementing Management Responsibility for Medical Devices brings together Device company Managers, Device Company Executives, Regulatory Affairs Managers, Quality Managers, Management Representatives, Risk Managers, Design Engineering Managers and Production Managers.