Spring brings: help with Clinical Investigations

 

The UK Clinical Submissions Process
 

We recently produced a series of six videos with the aim of providing guidance for the UK clinical submissions process on IRAS. Our Senior Clinical Associate, Claire Barclay, is very experienced in this area and is able to provide some helpful advice.

If you’re looking to initiate clinical investigations in the UK and have missed our video series, please do get in touch at info@psephos.com

 

You can watch all six videos on our website at https://www.psephos.com/clinical-services

 

MHRA Clinical Investigations Webinar

 

On 20th April, Psephos and SEHTA ran a free webinar session on "MHRA Clinical Investigations" with special guest Mark Grumbridge of the MHRA. The UK has always fostered a clinical research friendly environment aiming to advance disease diagnosis, medical therapies and improved patient care. With an increasing interest in medtech clinical investigations, the webinar provided an overview of the UK Medicines and Health products Regulatory Agency (MHRA) process for research clearance, advice and support.

If you were unable to attend, please get in touch with us below.

 
Contact us

MDR extension timings

 

If you'd like to discuss your EU MDR compliance, please contact

Jane or Marie at rep@psephos.com

Contact | Psephos Biomedica

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