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European Union Medical Device Regulation (MDR)

Find out more about the key changes of the new MDR.

What is MDR

The regulation applies to all Medical Device manufacturers who intend to place their medical devices on the European market. The EU Medical Device Regulation (MDR) will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC).

Key Changes due to New MDR

Explore and discover how the new MDR regulations impact your product lines. Set up one-on-one consultations with our experts and learn more MDR

Product Scope

UDI Implementation

Post Market Oversight

Common Specs

Reclassifications

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Clinical Evidance

Accountability

Clinical Evaluations

Re-certification

Business Benefits

Daily Compliance works across industries to provide guidance and support in auditing and compliance and provides below business benefits to you

Nearing a product launch? Learn more, how our services can help you!

General Info

info@thedailycompliance.com

-6203 San Ignacio Ave, Ste 110, San Jose, CA 95119

Phone – 515-708-6794

Platform

Digital Compliance Manager

Services

Product Design Reviews

Safety Test Lab Setup

Audit Consulting

Industries

Healthcare

Consumer Products

Technology