×

You're moments away from product development success!

First Name
Last Name
Company
Industry
Country
State
Province
Pending Opt-In
All fields are required. Your privacy is important to us.
Thank you!
Error - something went wrong!
   

EU MDR: What You Need to Know

The new EU MDR is a legal framework that includes three directives designed to regulate the safety of medical devices in Europe. These new regulations are far more comprehensive than previous regulations as the definition of a medical device now widely extends beyond what was considered a medical device in the past.

To get prepared and build safe, effective products that comply with these changing, more stringent MDR regulations, you’ll want to make sure your team is up to speed.

Download this eBook to learn:

  • What you need to know about the key MDR changes
  • The benefits of regulation revamping
  • How to implement the changes and achieve compliance with greater efficiency
Previous Video
Improving Quality Processes for Medical Device Development
Improving Quality Processes for Medical Device Development

In this webinar, our experts outline how Jama Connect can help you reduce risk and accelerate innovation in...

Next Flipbook
Accelerate Innovation in Medical Device Development
Accelerate Innovation in Medical Device Development

In this infographic, you’ll learn how Jama Connect can help accelerate innovation, maintain product quality...

×

First Name
Last Name
Company
Industry
Country
State
Province
Pending Opt-In
All fields are required. Your privacy is important to us.
Thank you!
Error - something went wrong!