Web-based data collection
tool
OnlineCRF

3 editions to cover all types
of clinical investigations

For clinical
trials

For the medical
devices investigations

For post-approval
studies

Why OnlineCRF perfectly
fits
small and medium sized
companies

In-built activity
tracking module

One quick view gives you a clear
picture
where is the study and which
study sites are not active

Fast startup

Four weeks from approved protocol
and
paper CRF to the start of data
collection

Full
validation pack

Skilled data management team will go
through the GCDMP-compliant
procedures
and prepare the full set of
validating
documents

Trainings,
consultancy
and support

All kind of support is included into the
price

Schedule live demo

Questions remain?

and our Data Manager
will contact you to answer

Useful links
to know
more about OnlineCRF

Features overview

The full list of DM activities

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