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QRC Consultants are experts supporting regulatory compliance for biotechnology and pharmaceutical companies in clinical drug development. 
Our focus is on Quality.

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QA and regulatory compliance

All aspects of Quality Systems Management and audit to support regulatory compliance for your clinical development programme, from Phases I - IV.

Regulatory affairs

A range of practical services to support your clinical development plans and agency interactions.

Advice and guidance on the ever-changing regulatory environments for conducting clinical trials

Clinical trial support

Comprehensive clinical research consultancy and monitoring services, including Ethics Committee submissions, Trial Master File Management, Vendor management and bespoke in-house training. 

latest news

Upcoming meetings

Meet representatives from QRCC at the following events:

11 October

BioForward - Roadmap for Growth, Life Sciences Event, Birmingham


6 November

RQA Annual Conference, Dublin, Ireland


In addition QRCC will be hosting a number of client focused meetings in Boston Mass. USA., during w/b 21 October 2019. If you would like to book an appointment to discuss your development needs please give us a call.





We are very pleased to announce the introduction of an electronic Trial Master File (eTMF) system.

QRCC have successfully implemented Veeva Vault, a cloud-based Content Management System, which is specifically designed to support life sciences organisations in managing essential trial documentation. The application is fully compliant with current industry standards, including the FDA's 21 CFR Part 11.

Our customers will now have the choice of utilising this system in support of their development projects.



Charity of the Month


QRCC are proud to support the Macmillan Cancer Support this month by hosting a "Bake Sale" here at the Silvaco Technology Centre in support of the Worlds Biggest Coffee Morning.


Macmillan provide valuable support and practical guidance to those whose lifes are affected by Cancer.



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