For decentralised or hybrid trials, or simple operational compliance and trial efficiencies, CRFWEB has the data collection modules you need.

Data from whatever source you require

CRFWEB’s approach to eSource marries our approach to managing the whole trial process. Everything you need, from whatever source you need, via whatever platform is required.

Direct Data Capture (DDC)

Fundamental to our eSource approach is allowing Direct Data Capture (DDC) via the CRFWEB app. Site staff can collect data at source, timed and verified directly onto the CRFWEB application. If they are out of range of a secure network signal, data will be held on the device and automatically synced.

Subject-led Data Capture

CRFWEB also allows data directly from the subject via our eDiary and ePRO modules.

Decentralised Clinical Trials

Together with our eConsent module, CRFWEB is an ideal integrated package for the provision of decentralised clinical trials.  Subject consent and remote data entry allow for the flexibility of fully decentralised trials or hybrid trials where part of the process or individual visits are handled remotely. This helps improve efficiency and subject enagement whilst speeding up the whole trial process.