DHF, DMR, DHR and TF - Regulatory Documents Explained 2013 is a webinar that covers topics such as:
- Design History File (DHF): Definition, Typical contents, DHF and outsourced design/production, DHF and OEM relationships
- FDA and MDD definitions/requirements
- Device History Record (DHR): Definition, Contents, Using DHR data for tracking and trending, DHR and outsourced design/production, DHR and OEM relationships
- Device Master Record (DMR): Definition, Typical contents, DMR and outsourced design/production, DMR and OEM relationships, Controlling and maintaining DMR
- Technical File (TF): Definition, Contents , TF and outsourced design/production, TF and OEM relationship
DHF, DMR, DHR and TF - Regulatory Documents Explained 2013 brings together:
- Production/Process Managers/Engineers
- Quality Managers/Engineers
- QA and QC managers, inspectors, supervisors and personnel
- Manufacturing Managers/Engineers
- Supplier Quality Managers/Engineers
- Documentation Specialists
- Regulatory Managers/Engineers
