Product
- JAMA CONNECT®
- Customer Success
Solutions
- Solution by Industry
- Solution by Function
- Compare
Company
- Company Information
- News and Events
  - Events
  - Press Room
Resources
Blog
Get Started
Search
Menu Menu

Satyajit Ketkar

Author Bio

Satyajit Ketkar talks about upcoming changes to the EU MDR regulation and what it will mean for your teams.

Recent Posts

All Posts

Recent Posts

An Interview with Velentium: How Medical Device Developers Can Prepare for EU MDR

on February 11, 2020 / in Compliance & Regulation / by Satyajit Ketkar

EU MDR which emphasizes patient safety, traceability, and transparency, will impact medical device developers, manufacturers, and suppliers across Europe.

CONNECT WITH US

Facebook
LinkedIn
Twitter
Youtube

USA
135 SW Taylor Suite 200
Portland, Oregon, 97204

EUROPE
Amsterdam Queens Tower
Delflandlaan 1, 1062EA Amsterdam
The Netherlands

© 2023 Jama Software

JAMA CONNECT
Product Overview
Pricing and Licensing
Success Programs
Trial

COMPANY
About Us
Careers
Customers
Press Room
Contact Us

RESOURCES
Resource Library
Events
Press Room
Blog
Success Programs
User Community
Support

Privacy Policy
Cookies
Privacy and Security
Legal
Preferences