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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


QRCC is delighted to welcome Samantha Whatling to the team as Snr QA Consultant.

Sam comes to us with a wealth of experience and will be supporting all aspects of QRCC's activities.



Charity of the Month

QRCC are proud to support Sue Ryder this month in memory of a very dear colleague who was cared for at the Thorpe Hall Hospice. 


The Sue Ryder organisation provides pallative and neurological support from specialist centres and in people's homes.


For more info: https://www.sueryder.org




A big thank you to all those who attended our recent Seminar here at QRCC.


"RSI (Reference Safety Information) and safety reporting" 


Topics included:

RSI and its relevance to clinical trial process, context/use

How to write & maintain RSI.

Implications of incomplete RSI, assessing impact & actions.

Agency interactions, CTA, GNA.

Common Inspection findings relating to RSI.


Plans are underway for our next event and full details will be posted shortly !





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