Quality, Regulatory and Clinical Consultancy
QRC Consultants are experts supporting regulatory compliance for biotechnology and pharmaceutical companies in clinical drug development. Our focus is on Quality.
Quality
All aspects of Quality Systems Management and audit to support regulatory compliance for your clinical development programme, from Phases I – IV.
Regulatory
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.
QRCC News
We are recruiting !
QRCC currently has a vacancy for a Clinical Trial Administrator to join the existing team based in St Ives. Please go to our Careers page for the full details of this role and be sure to contact us if you are interested.
QRCC’s Director and Head of Clinical Operations, Alex Gage, is appointed joint Chair of the CCRA’s Regulatory Affairs Working Group
The CCRA (Clinical & Contract Research Association) Regulatory Affairs Working Group was established early in 2021 with an initial mandate to support its members’ interests as follows: To keep a watching brief on the status of the current UK Government Trade...
