In postmarketing surveillance (PMS) studies, the doctor works with a large group of patients. To simplify the work of researchers, we use simple eCRFs.
An interactive tool for real-time monitoring. Dashboard helps with 3-click evaluate to see the dynamics of the study and find bottlenecks.
for data safety
All data is backed up every hour, and we store 24 subsequent copies on physically separate servers. In case of any problems or damage to the server, the data can be restored.
OnlineCRF allows the remote identification of “risky” sites and performing of some corrective or preventive actions.
3 weeks from approved Protocol and paper CRF to the start of data collection.
Safe data storage
The ability to choose a data center in accordance with the requests of the client. For example, we can select a safety data center close to your location.
Powerful and stable
The system collects data qualitatively, in a way that is stable and uninterrupted throughout the project duration.
Premium user support
Expert team will be responsible for user support. We provide quick feedback for requests during the clinical data collection period.
Head of Clinical
Olena has a master’s degree in pharmacy, and she has been working in the field of clinical research for over 2.5 years.
Olena oversees project managers in clinical trials. She organize the project team’s tasks and oversee the implementation of all study deadlines. Due to this, all project deadlines are respected, and all obligations to the client are fulfilled on time.