Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
2018 - Overview of Medical Device Regulation in Europe
Date2018-06-25
Deadline2018-06-22
VenueOnline event, USA - United States 
KeywordsClinical Trials; CERs; Medical Devices Directive
Topics/Call fo Papers
Areas Covered in the Webinar:
Introduction to Medical Device Regulation in Europe – background
Updates on the Regulations and their impact on CERs (Clinical Evaluation Reports)
How to design Clinical Trials, including how the MDR will affect post market clinical studies for existing products
Introduction to Medical Device Regulation in Europe – background
Updates on the Regulations and their impact on CERs (Clinical Evaluation Reports)
How to design Clinical Trials, including how the MDR will affect post market clinical studies for existing products
Other CFPs
- The Low-down on ACH and Regulation E
- Outcome Enhancement of Your Home Health Agency in 2018
- OSHA's New Injury Recordkeeping E-Submission Rule
- 2019 the 5th International Conference on Renewable Energy Technologies (ICRET 2019)--Scopus, Ei Compendex
- 2019 3rd International Conference on Energy and Environmental Science (ICEES 2019)--Ei Compendex and Scopus
Last modified: 2018-05-29 20:15:04