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 is 10 years old!
We are delighted to report that QRCC reached a significant milestone on the 2nd April 2022 by celebrating 10 years in business! Since commencing trading back in 2012 we have grown steadily to support our expanding portfolio of clients and now employ 18 staff across...
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QRCC has reached a significant milestone on the 2nd April 2022 by celebrating 10 years in business! We're looking forward to continuing to support current & new clients in the future & are working hard to ensure the next 10 years are as equally successful as the last.
Register for the combined review service. From 1 January it will be the only way to submit CTIMP applications: http://www.hra.nhs.uk/combined-review
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