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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.

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QRCC are pleased to announce the first in our 2019 Seminar series


“RSI (Reference Safety Information) and safety reporting” will be held on 21st March 2019 at our premises in St Ives, close to Cambridge. 


Topics will include:

Introduction – 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.


Registration fee: ÂŁ180 + VAT




Charity of the Month


QRCC are proud to support The Samaritans this month.

The Samaritans run a 24 hour/day, seven day/week phoneline to support people in need, of all ages and from all walks of life. They also run a number of campaigns to raise awareness of their work and highlight how we can all help the people around us by simply being prepared to listen. 

January can be a particularly difficult month for a lot of people for various reasons and we are pleased to support this worthwhile charity with our fundraising efforts.

The Samaritans is a charity and it’s the public’s donations and the work of more than 20,000 trained volunteers that mean they are always there for anyone struggling to cope.   

For more info: http://www.samaritans.org/support-us




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