QRC Consultants are experts supporting regulatory compliance for biotechnology and pharmaceutical companies in clinical drug development.
Our focus is on Quality.
All aspects of Quality Systems Management and audit to support regulatory compliance for your clinical development programme, from Phases I - IV.
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
Comprehensive clinical research consultancy and monitoring services, including Ethics Committee submissions, Trial Master File Management, Vendor management and bespoke in-house training.