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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 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  ! 

 

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Upcoming meetings

 

QRC Consultants are attending the following upcoming events:

29/30 Jan 2020 CCRA - Professional Awareness Update meeting, London

13 Feb 2020 MHRA- GCP Symposium, London

 

Charity of the Month

 

This month QRCC are proud to support GAIN, a charity that offers help and support to those affected by Guillain-Barré & Associated Inflammatory Neuropathies. These diseases can have a devastating effect on those diagnosed and their family and friends. Help is available from GAIN for everyone, whether you are the patient or close to someone who has been diagnosed

 

For more information visit : https://gaincharity.org.uk/

 

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eTMF

 

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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