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 attending EUCROF24 congress
Alex Gage, QRCC's Director & Head of Clinical Operations, will be attending the EUCROF24 congress in Prague on the 19th and 20th February. Alex is looking forward to connecting with colleagues across Europe and talking about how QRCC can help companies with their...
QRCC Sponsor Oversight Virtual Seminar
Following on from the success of our in-person Sponsor Oversight seminar held at the end of November, we are happy to announce that we will be holding a virtual version of the seminar in Q1 2024 to allow our colleagues and clients based further afield and ex-UK to...