MDR definition

MDR means Managed Detection Response.
MDR means the person appointed by the Beveridge Joint Venture to perform the function of the Mandalay Design Reviewer in accordance with the Design and Siting Guidelines and Restrictions.

Examples of MDR in a sentence

  • MDR is a broad new framework of regulations for medical device manufacturers that is mandatory from May 2021.

  • As with everything else MDR has been impacted by Covid-19 by travel restrictions and a shortage of resources at our approving authority (‘no- tified body’), TÜV SÜD.

  • Several research projects and clinical studies for both Non-Melanoma Skin Cancer (NMSC) and the barrier application have been slowed or de- layed, and our MDR approval, though progressing, has taken much longer than expected.

  • MDR update As we have received a number of questions from shareholders around the Medical Device Regulation (MDR) process, I thought I would update you on our status in some detail.

  • The project’s legal experts have analysed the EU Medical Device Regulations (MDR), General Data Protection Regulation (GDPR) and the upcoming EU AI-Act and extracted a total of 15 requirements.


More Definitions of MDR

MDR means Ministère du Développement Rural, the Borrower’s Ministry of Rural Development;
MDR means Mastech Digital Resourcing, Inc., a Pennsylvania corporation.
MDR means a report filed with FDA to communicate an event when Seller or Buyer becomes aware (as such phrase is defined in 21 CFR 803.3(c)) of information that reasonably suggests that one of its marketed Products:
MDR means “Managed Detection and Response,” (formerly known as “BDR” meaning “Breach Detection and Response”) which is a module available in the Defendify platform that incorporates 24/7 device and network cybersecurity monitoring, detection response and containment along with reporting and advisory professional services.
MDR means Medical Device Reporting as defined by FDA
MDR means medical device re- port.