Blood Sciences Research
What is a CTiMP study - A Clinical Trial of an Investigational Medicinal Product is a study that looks at the safety or efficacy of a medicine/foodstuff/placebo in humans, as defined by the Medicines for Human Use (Clinical Trials) Regulations 2004. The Medicines and Healthcare products Regulatory Agency (MHRA) is the government agency which is responsible for ensuring that medicines and medical devices work, and are acceptably safe.
How to get involved (including flowchart) Done - flowchart produced (registration of studies)
Meet the Team & contacts / site visits
Helena Baker (Biomedical Scientist) - 0113 3922915 Email: leedsth-tr.pathologyRD@nhs.net
Conor O’Malley (Operational Lead) - Tel: 0113 3922544 Email: conor.o'malley@nhs.net
Dr Carys Lippiatt (Consultant Clinical Biochemist and Clinical Lead) - 01132067174 carys.lippiatt@nhs.net
Accreditation / UKAS calibration certificates / UKAS temperature monitoring
Hyperlinks to UKAS calibration certificates for: pipette, centrifuge, balance, temperature sensors (links to EQMS - documents currently uploaded to the latter)
Hyperlinks to UKAS schedules of accreditation on website for each department
Feedback section - please send feedback to leedsth-tr.pathologyRD@nhs.net
