Product Overview
Specially designed for small and medium companies
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.
- 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.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
OnlineCRF fits a variety of trial and study designs
Clinical Trials I-IV phase
- - Randomized/non- randomized;
- - Blinded/unblinded;
- - Stratified;
- - Comparative, crossover;
- - Single or multi-country;
- - Long and short term.
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.
Medical Device investigations
- - Fast start - up to 4 weeks;
- - Cost-effective solution;
- - Integration with medical device possibility;
- - Self-evident interface.
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.
About the company
OnlineCRF is a vendor of EDC systems for conducting clinical trials.
Our experience of the actual clinical trials and postmarketing studies have given us a clear understanding of the needs of CRO and pharmaceutical companies in clinical data collection.
Among other things, we saw that small companies do not always have the ability to maintain a Data Management department. Therefore, we created an EDC system that is fully configurable for the client by our Data Managers. There is no need to hire data managers or outsource EDC configuration to other companies. You will get ready-to-go EDC, which is completely configured in strict accordance with the study protocol. Just log in and manage your clinical study.
An all-in-one solution gives you an easy, fast, and cost-efficient way to perform clinical data collection.