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.
Comprehensive clinical research consultancy and monitoring services, including provision of bespoke in-house training seminars, and periodic updates on the ever-changing regulatory environments for conducting clinical trials.
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QRCC are proud to support Sue Ryder this month in memory of a very dear colleague who was cared for at the Thorpe Hall Hospice.
The Sue Ryder organisation provides pallative and neurological support from specialist centres and in people's homes.
For more info: https://www.sueryder.org
A big thank you to all those who attended our recent Seminar here at QRCC.
Topics included:
RSI and its relevance to clinical trial process, context/use
How to write & maintain RSI.
Implications of incomplete RSI, assessing impact & actions.
Agency interactions, CTA, GNA.
Common Inspection findings relating to RSI.
Plans are underway for our next event and full details will be posted shortly !
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