Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs 2014 is a webinar that covers topics such as:
- Corrective And Preventive Action (CAPA) And Complaint Files
- Device History Record (DHR) And Device Master Record (DMR)
- Definitions
- Applicable Laws
- Frequent Citations in 483s and How to Avoid
- Quality System Procedures, Purchasing Controls And Servicing
- FDA Quality System Regulations
- Process Validation
- Top 20 Items Cited in 483s
- Design History File (DHF)
- Mistakes While Implementing QSRs
- Inspection, Measuring And Test Equipment
- How to Avoid Mistakes
- Quality Requirements For Premarket Approval (PMA) Application
- Design Control: Design And Development Planning, Design Input, Design Output, Design Review, Design Verification, Design Validation, Design Transfer, And Design Changes
Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs 2014 brings together VPs, CEOs, Attorneys, Compliance Officers, Managers (RA, QA/QC, CA), R&D and Manufacturing Managers, Contractors and Subcontractors and Consultants.
