diCELLa eCRF clinical trials is a web application, which provides creating and managing CRF, in non-commercial clinical research. The application is for both – Sponsor/CPO and research group. The data in diCELLa eCRF clinical trials are protected for non-authorized changes by blockchain technology, which provides non-repudiation.
diCELLa eCRF clinical trials is a web application, which provides creating and managing CRF, in non-commercial clinical research. The application is for both – Sponsor/CPO and research group. As a Reasearch Sponsor You will be able to create CRF for new clinical reasearch in a quick way, follow research’s realization progres and do monitoring visits. As a research group You will be able to fill a CRF of research participants.
The data in diCELLa eCRF clinical trials are protected for non-authorized changes by blockchain technology, which provides non-repudiation.
diCELLa eCRF clinical trials is dedicated to non-commercial clinical research in early phase, with a large share of researchers in a project stage.
eCRF clinical trials is compatible with a tissue donor’s qualification according to legislation from 1st of July 2005 about collecting, storaging and transplantation of cells, tissues and organs, which makes work with autologous medical products easier.
Research group: diCELLa eCRf clinical trials has a research group, monitor and sponsor structure.
Sponsor/CPO: eCRF clinical trials will let for CRf preparing for new clinical research and managing tchem in a easy way.
diCELLa eCRF clinical trials provides easy printing eCRF elements, period reports about donors and tissues/cells.
