Projects for successful approval
of medical devices
OnlineCRF helps collect clinical evidence for obtaining certification accordance with MDR regulation. Projects that will be powered by OnlineCRF:
Post-Market Clinical
Follow-Up (PMCF) studies
You can involve to study clinical hospitals from any country and any district.
Studies
for MDR registry
OnlineCRF can be configured for long-term data collection as an essential part of the product registry process.
Clinical trial
for medical devices
OnlineCRF empowers different medical-device trials, supporting files upload and commenting (DICOM etc.).
OnlineCRF complies
with the industry standards
Why we differ
Fast startup
2 weeks from approved Protocol and paper CRF to the start of data collection.
No heavy load for your team
We only need up to 8 hours of your time to produce a ready-to-go EDC system. All other preparation processes are undertaken by our team.
Cost-effective
solution
The ability to configure the EDC system even for low-budget projects.
Any type of data
can be collected
It is possible to collect any type of data that you need: safety signals, medical images, information about patient and doctor atisfaction, etc.
Responsible for EDC system stability and availability
Vasiliy Vinnikov
System Configuration
Manager
Vasiliy is an IT specialist. He has been working in this field for more than 4 years. Of these, over 2 years have involved clinical data management and tuning data collection systems. Vasiliy is responsible for configuring the OnlineCRF electronic system in accordance with project requirements. In addition, Vasiliy is responsible for validating and testing the system. Thanks to his work, the client receives a convenient system that has all the functions necessary for conducting research on medical devices.
