The Basics of US Medical Device Regulation 2015 is dedicated to basics of US Medical Device Regulation.
Key Topics
Post marketing
CAPA
QSR
Inspections
Reporting
Export for foreign markets
Clinical Trials
Other
IDE
Common problems in trial design and management
Export for trials
Who should Attend
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
Past Events
Basics of US Medical Device Regulation 2015 - 17-18 Dec 2015, DoubleTree by Hilton Hotel San Francisco Airport, Burlingame, California, United States (48681)
Basics of US Medical Device Regulation 2015 - 19-20 Feb 2015, Courtyard Boston Logan Airport, Massachusetts, United States (48682)
Basics of US Medical Device Regulation 2026
Important
Please, check "Basics of US Medical Device Regulation" official website for possible changes, before making any traveling arrangements
