One quick view gives you a clear picture where is the study and which study sites are not active
Four weeks from approved protocol and paper CRF to the start of data collection
Skilled data management team will go through the GCDMP-compliant procedures and prepare the full set of validating documents
All kind of support is included into the price
Outsource all EDC
related tasks to us and save your company’s resources.
Don't care about EDC configuration
Get a ready-to-go data collection tool for any project in addition to a full set of GCDMP-compliant documentation.
Manage multiple clinical trials
and easily delegate tasks to our data managers, coders, and remote monitors.
Data is stored in a secure environment
with incremental backups in a data center close to you.
Get the EDC system
that strongly meets the Protocol and CRF requirements.
The full set of validation documentation
in accordance with regulatory requirements.
Fully prepared EDC system for your trial.
You do not need to study multi-page manuals to configure eCRF. Just log in and start the data collection!
fast startup (4 weeks), documentation, technical, and user support are included.
OnlineCRF is a perfect fit
for interventional and PMCF studies.
Get a cost-effective EDC system
for low-budget projects.
OnlineCRF helps to collect data quickly
and speed-up the device’s time-to-market.
OnlineCRF is simple and intuitive
It is highly important to collect data of good quality with no need for extensive training.
OnlineCRF provides cost-effective solutions
for small projects.
Get a fully prepared EDC system for your research
The system is ready to work according to your particular project, and you do not need to configure anything.
Get your system ready in 4 weeks
You can start your project without delay.