GCP Clinical Processing
Following approval of the analytical validation process by our QA Team and the Responsible Scientist the assay is ready for use in GCP processing studies.
During clinical processing all critical steps and transfers are witnessed by a 2nd Operator to prevent laboratory errors. Once complete, the data and reports are approved and released by QA and the Responsible Scientist. All GCP projects can be run as rapid response studies to allow return of data in a matter of hours. Tepnel’s GCP compliant service is a fully bespoke service such that we can accommodate any requirements for e.g. data and report formats.