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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.

Clinical trial support

Comprehensive clinical research consultancy and monitoring services, including provision of bespoke in-house training seminars, and periodic updates on the ever-changing regulatory environments for conducting clinical trials.

latest news



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 be supporting MIND, the mental health charity, this month.


Mind offer advice and support to empower anyone who is experiencing mental health problems and campaign to improve services, raise awareness and promote understanding of mental health.

Statistics suggest that one in four people in the UK will experience a mental health problem in any given year.

Mind rely entirely on public donations to fund their activities.


For more info: https://www.mind.org.uk/




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