The application is designed for both the Study Sponsor/CRO and the research team. As a study sponsor (and/or CRO), you will quickly create a CRF for a new clinical trial, be able to keep track of the progress of the clinical trial and make monitoring visits. As a research team, you will be able to easily complete CRFs of study participants.
The data in diCELLa CRF Clinical Trials are protected from unwanted changes through BLOCKCHAIN technology, ensuring authenticity and non-repudiation.
diCELLa eCRF clinical trials is dedicated to non-commercial early-phase clinical trials with strong investigator participation at the trial design stage.
The eCRF clinical trials is compatible with tissue donor qualification under the Act of July 1, 2005 on the Collection, Storage and Transplantation of Cells, Tissues and Organs (along with implementing acts), facilitating work with autologous medicinal products.
Research team: diCELLa eCRF clinical trials reflects the structure of the research team, monitor and sponsor in a clinical trial.
Sponsor/CRO: eCRF clinical trials will allow CRFs to prepare for new clinical trials and easily manage ongoing trials.
diCELLa eCRF clinical trials in any eCRF component can easily print periodic reports on donors and collected tissues/cells.