Online CRF System | Electronic Data Capture (EDC) system for clinical trials

Online CRF

Electronic Data Capture (EDC).

Designed for small and medium companies clinical trials.

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Delegate any EDC-related tasks to our team

Higher standards

Our Services

User Friendly and Easily Manageable System

Follow All Patients in Online

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True flexibility

We can implement non-usual features or unique project-specific requirements. It is even flexible from a budget perspective: the EDC system is perfectly fitted to low-budget clinical research.

Fast start-up

EDC system OnlineCRF is ready to go within 4 weeks (from approved Protocol and CRF). Send a request, and you will get feedback in 8 working hours. Check our speed right now.

Data safety

The EDC system source code and the database are stored in the European datacenter or in any other country that you choose. The safety of clinical data is also guaranteed by the multilevel backup.

Saving your time

The Electronic Data Capture tool is fully configured by our team and perfectly complies with your project needs. Do not spend your valuable time on system configuration and validation.

Multilanguage

Interface can be rapidly translated to any language (only one language supports by one instance)

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Data Export

Data are exported at any time in SAS-compartible format. Populated CRFs can be saved as PDF

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Related services

If you need services related to clinical data management (in addition to a fully-configured EDC system), we have a set of services specifically for such cases.Our services will be useful to you, for example, in cases such as:

you have an EDC system from another provider (not OnlineCRF), and you need to configure it and get data management support for that;
you need to outsource any number of data management activities in your clinical trial;
you need a remote data management command for several projects, etc.

Book Appointment

10000+

Patients

1520+

Active User

50+

Countries

400+

Clinics

We are working for:

Clinical Research Organisations(CRO)
that strongly meets the Protocol and CRF requirements.
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Biotech/Pharma Companies
in accordance with regulatory requirements.
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Clinical Trial Investşgators
You do not need to study multi-page manuals to configure eCRF. Just log in and start the data collection!
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Medical Device Companies
fast startup (4 weeks), documentation, technical, and user support are included.
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Key employees

Our company is inspired by the idea of developing an innovative tool for clinical data collection. We constantly remember that valuable data is collecting via CRF.Digital to improve the treatment of various diseases and help thousands of people.