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
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...
QRCC upcoming meeting attendance
QRC Consultants will be attending the following Industry events: The ICR Ethics & GCP Forum, March 18th, 2021 (Online) OBN BioLearn, March 24th, 2021 (Online) European QA Symposium, May 20-21, 2021 (Online) You are welcome to introduce yourself to us at any of...
