Master Production Record Requirements - Webinar By GlobalCompliancePanel 2011 is a webinar that is focused on Roles and Responsibilities, Device Master Record (DMR), Issuance of BPR, Content of the MPR, Review and Approval of MPR, Creation and Revision of Master Production Record (MPR), Regulatory Expectation (FDA and EU).
The event brings together:
- Maintenance
- Regulatory Affairs
- Quality Control
- Materials Management
- Validation
- Quality Assurance
- Manufacturing
