The Basics of US Medical Device Regulation 2015 is dedicated to basics of US Medical Device Regulation.
The Basics of US Medical Device Regulation 2015 covers topics such as:
- Post marketing
- CAPA
- QSR
- Inspections
- Reporting
- Export for foreign markets
- Clinical Trials
- Other
- IDE
- Common problems in trial design and management
- Export for trials
The Basics of US Medical Device Regulation 2015 brings together:
- People who are Interested in Starting a Company to Sell Health-related Products
- People who are Working in non Regulatory or QA Areas of Medical Device Companies
- People who are Interested in Selling Medical Devices
- People who are Interested in financing a Health Care Company
