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 Seminar 30th November 2023
We are pleased to announce that registration is now open for the first QRCC seminar since COVID-19, titled “Sponsor Oversight of Outsourced Clinical Trials”. This seminar will focus on the Sponsor oversight responsibilities as set out in the draft of ICH E6 R3 (the...