THE MOST FLEXIBLE EDC FOR ALL YOUR STUDIES
- Randomized Clinical Trials
- Case-control studies
- Electronic Patient Reported Outcomes (ePRO)
- Electronic Clinical Outcomes Assessment (eCOA)
- Administrative clinical databases
- Cross-sectional studies
- Patient and physician web surveys
- Cohort studies
- Patient registries
- Patient diaries
- Observational Studies
- Chart Review Studies
- Post-marketing studies
- Web Surveys
TOP FEATURES
- Configurable web interface
- eConsent form with signature
- Image based data entry
- Advanced validation rules and edit checks
- E2B for pharmacovigilance
- Upload & download files
- Skip patterns (visible or enabled)
- Drop down list filtering & searchable lists
- Table designs (static and dynamic)
- Registry designs with higher level grouping events
- eDiary capabilities (daily or hourly)
- Visit scheduler email and phone reminder tracking
- Secure fields to authorized users only
INDUSTRY STANDARDS
PARTNERSHIPS
WHAT CLIENTS ARE SAYING ABOUT US
We have been using Dacima for a clinical trial, and needed a full audit trail to comply with FDA guidance for clinical trials. Dacima is a small Canadian company, and it has been a pleasure to work with them on our trial. Their system is most appropriate for longitudinal studies, as it can fully integrate a range of study components longitudinally. Our trial with Dacima is fully integrated into their system, including automated text (SMS) reminders for study visits, electronic consents, electronic CRF, enrollment, randomization procedure, and participant surveys. Dacima’s services were able to fit within an NIH budget for our clinical trial, and they have provided our team at Emory with a fully featured system that meets all our need for the trial. They also have been very responsive in developing functionality particular to our study. I think this is in part because the CEO has a PhD in Epidemiology, so he understands the needs of academic institutions in implementing clinical trials. In sum, I highly recommend Dacima.
Control, ease of use, cost — DACIMA provided a one-stop solution for our clinical data collection: – Control of all aspects of the study / registry from your own offices – Cost is very low compared to other customized solutions – Easy to make edits and duplicate forms – When needed, programmer support is quick and excellent – Wide range of variable types and dependencies – Lots of user control and permission settings – We’ve had good feedback from doctors that the interface and forms looked very professional – Instant compliance with required data management requirements
I’ve been using the software for about 3 years until now, and it helped my team to build up very powerful eCRFs. Our clinical studies became easier to follow. Furthermore, using DACIMA Software helped the investigators to be more efficient at the patient enrolment and monitoring. The alert procedures are very supportive. Moreover, our data manager is closely assisted in forms building.
Dacima offered us a solution tailored to our unique needs, which included limited internet access, inexperienced data entry personnel, a bilingual interface, project-specific data reporting forms and security requirements. Dacima has provided outstanding service. I give Dacima Software my highest recommendation and sincere admiration for its professionalism and dedication to providing work of the highest quality.
I have been a Dacima Software client for more than three years. It has been a great partnership. The Dacima Software people have demonstrated that they are good listeners, action-oriented and client-friendly. I am very pleased with their software and the changes that they have made in response to the changing Study needs.
I have used DACIMA for over 5 years and the platform meets the regulatory requirements needed to support a high standard academic trial. Using DACIMA services is affordable even with an academic budget. The customer service is above expectations.