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What is the difference between the EN and ISO versions of 14971:2019? Part 1
14th September 2020

What is the difference between the EN and ISO versions of 14971:2019? Part 2
14th September 2020

Is Analysis of Multiple-Fault Conditions a Requirement of ISO14971?
14th September 2020


EU MDR - One Year Delay is Proposed by the EU Commission

One Year Delay to EU MDR is Proposed

Written by John Lafferty

Read Time (1 minute)

The EU Commission is proposing to the European Parliament that the new EU MDR be postponed by one year in order to allow the industry and relevant authorities to concentrate on priorities related to the Covid19 pandemic. This information was published via a video by Mario Gabrielli Cossellu, Policy and Legal Officer at European Commission on March 25th 2020. 

Video Transcript 

"The Commission is working on a proposal to postpone the entry into force of the new Medical Devices Regulation for 1 year. We are working hard to submit this proposal early April and we call on Parliament and on Council to adopt it quickly as the deadline for entry into force is at the end of May. This will relieve pressure from national authorities and industry and it will allow them to focus fully on urgent priorities related to the coronavirus crisis". 

Link to the Video 

Ongoing updates 
In the months ahead, Northridge Quality & Validation and our training partners SQT Training Ltd. will bring you further updates on relevant developments in the industry. 

Virtual Training Courses  
Northridge Quality & Validation and our training partners, SQT Training run a range of training courses for the industry. Note: Courses will be delivered via a Virtual Classroom (not in person)Courses will available by virtual classroom delivery from April 2020 onwards so that you can attend the course without leaving your office or home. Find details of upcoming courses here. 


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