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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


We are delighted to welcome Adele Steele to the Quality team here at QRCC.

Adele joins us a QA Consultant having worked in the pharmaceutical industry for more than 25 years.



We are recruiting !

QRCC are seeking an experienced GCP QA auditor to join the team based in St Ives, UK.

The ideal candidate for this role will have clinical QA experience, including auditing and an understanding of the regulatory environment for the conduct of clinical trials.

Interested in this role ? Go to our Careers page for more details  ! 




Upcoming meetings

Alex Gage of QRC Consultants will be presenting at the Veeva R&D Summit - Europe being held in Barcelona between 18-20 May 2020.

Check out the programme here: 


We look forward to seeing you there !




Charity of the Month


This month QRCC are proud to support Alzheimer's Research UK, a charity that offers help and support to those affected by dementia.This disease can have a devastating effect on those diagnosed and their family and friends. 

Alzheimer's Research UK also funds pioneering research projects and is dedicated to making life-changing breakthroughs in diagnosis, prevention, treatment and cure through investment in research


For more information visit : https://www.alzheimersresearchuk.org






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.



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