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 Christmas Opening Hours
QRCC would like to thank our clients and collaborators for their continued support in 2024 and to wish you all every success with the fresh opportunities that 2025 may bring. QRCC will close for Christmas on 24 December 2024 and will re-open on 02 January 2025.
QRCC Sponsor Oversight Virtual Seminar
We are pleased to announce that registration is now open for the virtual QRCC seminar titled “Sponsor Oversight of Outsourced Clinical Trials”. This seminar (a virtual version of the in-person Sponsor Oversight seminar held last year), will focus on the Sponsor...