FAQs

What is Sarah Cannon Research Institute UK ?

Sarah Cannon Research Institute UK have partnered with the Leaders in Oncology Care (LOC), the largest provider of private oncology services in the UK, to open the first private oncology drug development unit in the country. Our state of the art facilities cover 13,000 square feet and provide a premier patient experience - to both NHS and privately insured patients.

What are your timelines for R&D approval ?

Five working days from receiving all approved study documents (MHRA, REC, Budget/Contract etc.).

Does your site have experience using Electronic Data Capture (EDC) ?

Yes. Our staff has experience using a number of different EDC systems such as InForm, Medidata Rave, Oracle and Trial Master.

Will your site finalise the contract and budget prior to regulatory submissions ?

No. The contract and budget are finalised in parallel with regulatory submissions in order to expedite the setup process.

Will the study monitor have internet access during monitoring visits ?

Yes. Wireless internet access is available.

Does your site use Electronic Medical Records ?

Yes. However, information regarding trial patients is printed, signed and dated, then filed in individual patient clinical trial folders which the monitor will review.