eCRF.bizTM system leaves traditional, paper documents aside (case report forms, profiles, etc.) created and gathered in the course of the research project. It allows to collect data remotely, data management as well as it includes an analytical module, which allows to monitor progress and generate project statistics.
Thanks to the implementation of the newest analytical solutions, it eliminates the risk of missing data in an effective way. This system contains an automatic record control component which supports the correctness verification process even at the stage of data implementation
Access to the gathered information about patients.
Statistics of the data collected(summative charts, graphs).)
Research progress statistics (simple, dedicated).
Possibility of printing out the filled-in CRF forms.
Possibility of printing out AE/SAE forms, e.g. CIOMS.
Audit trail – Monitoring the changes in the values recorded.
Data query - Mechanism of querying.
Mailing - Sending e-mails about adverse events.
This module ensures an efficient and flexible process of patient randomisation which allows to define necessary functions in order to conduct a reliable clinical trial. This module is compliant with FDA standard: 21 CFR Part 11.
The drug management module monitors the medical supplies among distribution centres, ensuring availability of proper resource in order to ration them to patients.
Online contracts not only guarantee optimised and shortened process of contracting but also the utmost comfort and absolute safety. Thanks to online signing, we reduce the amount of needless printout as well as we avoid the necessity of sending documents via post or couriers. It speeds up the contracting process, reducing thereby the amount of time needed for the documents to be delivered as well as it improves the ways of accounting with the researchers or signing possible annex – in case of prolonging research.
The contracting process has never been so easy. All you need is to:
Observational research with the use of eCRF.bizTM system is carried out in compliance with the guidelines included in Standard Operating Procedures.
Authorial editor guarantees a number of options which facilitate creating forms in a quick and easy way. The creator allows to set conditions between queries, sites and particular fields by Drag&Drop option