Accelerate clinical data collection
As intuitive and easy to use as a paper CRF
Design and build with no coding skills

Discover how to finish your clinical studies in less time

by avoiding mayor headaches with our eCRF with integrated ePRO.

Keep your study under control

Success stories

The main advantages of ShareCRF is the speed with which we can implement the solution and the fact that we don't really need internal or specialized staff to do it and maintain it.

Iker Navarro CEO | Noorik Biopharmaceuticals

The main benefits are lots of time saving, it's easy to introduce the data and it's really fast to export the data and from that on to analyse the data obtained in the studies.

Rita Carilho Torrao Project Manager | Scientific Affairs | CETERA

One of the biggest improvements we have perceived is the reduction in monitoring times as well as in the times to validate data in the eCRF.

Mercedes Ramas Clinical Operations Manager | QualitecFarma

What I like the most is the capacity to adapt to the needs I have at every moment, even during the study, not just at the beginning of it.

Javier Fernandez García Project Manager | Clínica Universidad de Navarra

Do you still use paper?

You can’t consult in real time.

You will have to do a double data entry so have your data in digital format.

You will have several expenses that are usually not taken into account.

Do you use Excel or similar?

Hard to use and has a greater risk of error by the users

It will be complicated to unify different files from different sites.

Complying with the regulatory norms will be highly complicated (Audit Trial)

Very complicated to monitor.

Do you use a custom-developed application for your study?

Implementation time for the project will be larger and the launch time for the study will be delayed.

The cost will be greater: dedicated specialists, full validation of the tailor-made software, dedicated servers, etc.

Any changes in the study once it has already begun will be slow to make, because of the change itself and for the complex validation required.

Are you using a configurable EDC? Make sure you use the right one.

Easy and intuitive for the users.

No need for coding skills

With a secure and easy to use system to make changes mid-study.

A properly validated platform that complies with regulatory norms.

With support that actually works

Design the CRF with no coding skills whatsoever

Changes mid-study? No problems and in minutes

Comply with all the norms without going crazy

Save time in monitoring and data validation

Automatic pilot randomization

Cloud solution. Forget about managing servers

Stop using paper forms for the participants in the study

Choose who can access each data and encrypt significant data

As intuitive and easy to use as paper

Stay updated on the most important events

Allow investigators to include files as patient data

Clean data with no mistakes, on the first try