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Electronic Data Capture (EDC) system
for clinical trials

Specially designed for small and medium companies

Patient’s data

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Data gathering

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Data entry

EDC system

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Delegate any EDC-related tasks to our team. You can invest your time in what is important

We know that clinical research requires a lot of attention and time. This places a heavy load on the project team, and there is a big challenge to manage everything.

We tailored the solution to save your time in tasks related to Electronic Data Capture in clinical trials. Our data management department creates everything you need to properly collect clinical data. This will help free up your time for what is important.

We are working for:

OnlineCRF_EDC_system OnlineCRF_EDC_system_mobile

OnlineCRF fits
a variety of trial and study designs

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Clinical Trials

I-IV phase
  • - Randomized/non- randomized;
  • - Blinded/unblinded;
  • - Stratified;
  • - Comparative, crossover;
  • - Single or multi-country;
  • - Long and short term.
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Postmarketing studies

Non-interventional
  • - Observational, epidemiologic, retrospective;
  • - Large-scale: up to 300 sites, up to 50 000 subjects;
  • - PAES, PASS, DUS;
  • - Single or multi-country.
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Medical Device investigations

  • - Fast start - up to 4 weeks;
  • - Cost-effective solution;
  • - Integration with medical device possibility;
  • - Self-evident interface.

Why OnlineCRF?

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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.
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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.
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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.
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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.

OnlineCRF complies
with the industry standards

fda
ispe
scdm
eu

Case studies

Prostate cancer drugs III phase

pepti
  • - Interventional study
  • - 35 sites
  • - 8 countries
  • - 184 patients

Responsible for the project success

bystrov_roman

Roman Bystrov
Head of Data Management

Non-alcoholic fatty liver disease

sanofy
  • - Non-interventional study
  • - 100 sites
  • - 5,000 patients

Responsible for the project success

tkachuk_elena

Olena Tkachuk
Head of Clinical Operation

Our beloved clients

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