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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


QRC Consultants - response to COVID-19 infection

QRCC has taken appropriate measures to ensure that it can continue to operate as usual in supporting its customers.

We are implementing some logistical changes in line with the latest guidance from the UK government and this will include remote working. 

We have also taken the decision to avoid any business travel and face to face meetings.

All meetings and general communications will continue via the usual channels of e-mail, telephone or teleconference.

Our central office number will be manned during normal business hours and all our consultants will be contactable via their mobile numbers.  






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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