7 easy steps for building your ObTiMA trial
ObTiMA allows you to focus on your research needs and requirements.
Our Services
We help researchers to design and conduct clinical trials!
Step 1 - Trial Design
Design your trial according the ontology based structure with data logic support and version management
Step 5 - Create Sites
Add sites to your trial according your protocol
Step 2 - Create CRFs
Define your CRF layout, data structure, use dynamic capabilities or reuse forms and data elements from CRF repository.
Step 6 - Register subjects
Include, exclude otr enroll subjects with dynamic eligibility checking
Step 3 - Create Events
Define event type (scheduled, unscheduled, repeating, etc.) and select CRFs that are associated with the event
Step 7 - Conduct trial
Electronic Data Capture with data input, modification, validation, export, etc.
Step 4 - Create Users
Create trial users and manage their access privileges