Dacima Clinical Suite
About Dacima Clinical Suite
Dacima Clinical Suite is a clinical data management software from Dacima Software that supports the management of clinical trials and research studies. It includes data collection tools, real-time reporting, and regulatory compliance features so researchers can efficiently manage their clinical data. The suite is designed to facilitate electronic data capture (EDC) and offers user-friendly interfaces for data entry and monitoring. Key capabilities: data collection real-time reporting regulatory compliance user interface customization multi-site management Best for: clinical researchers and trial managers that need a comprehensive solution for managing clinical trial data.
Dacima Clinical Suite by Dacima Software is a comprehensive electronic data capture (EDC) and clinical trial management system (CTMS) designed to streamline clinical trial data collection processes. Its primary purpose is to enhance the management of clinical trials by providing tools for efficient data capture, validation, and reporting. With interactive dashboards, CDISC-compliant form libraries, detailed reporting functions, and robust data validation tools, Dacima Clinical Suite helps clinical researchers and organizations optimize their workflows and ensure compliance with regulatory requirements. The user interface of Dacima Clinical Suite is intuitive and user-friendly, featuring a clean and modern design with easy navigation that makes it accessible for users of all technical skill levels. Interactive dashboards, customizable reports, and real-time analytics enhance the overall user experience. The platform also provides various learning formats, including video tutorials, webinars, and documentation, to support users in getting accustomed to the software efficiently. Dacima Clinical Suite offers an extensive set of functionalities that set it apart from its competitors.
Pros & Cons
- +• Affordable: Offers a cost-effective solution, especially compared to other custom EDC options.
- +• User-Friendly: The interface is intuitive and easy to use, even for beginners.
- +• Customizable: Highly flexible, allowing for tailored eCRF design and study-specific functionalities.
- +• Excellent Support: Provides responsive and helpful customer support, often involving the CEO directly.
- +• Comprehensive: Integrates various study components, including eCRFs, randomization, ePRO, and reporting, into one system.
- +• Compliant: Fully compliant with regulatory requirements like Title 21 CFR Part 11.
- −• Requires Support for Some Changes: Users may need technical support for certain complex modifications, although response times are quick.
- −• Minor Interface Quirk: Saved changes on forms can cause the page to jump to the top, disrupting workflow slightly.
Features
Key features
- 1. Flexibility
- Suitable for a wide range of study types, including randomized clinical trials, observational studies, registries, eCOA/ePRO, and more.
- 2. Configurability
- Web interface, forms, and workflows can be tailored to specific study needs.
- 3. eConsent
- Includes electronic consent forms with signature capture.
- 4. Advanced Validation
- Features robust data validation rules and edit checks.
- 5. eDiary Capabilities
- Supports daily or hourly patient diary entries.
- 6. Compliance
- Meets industry standards, including FDA guidance and E2B for pharmacovigilance.
- 7. Affordability
- Cost-effective solution, even for academic budgets.
- 8. Excellent Support
- Responsive customer service and technical support, with expertise in clinical trial needs.
- 9. User-Friendly
- Easy to learn and use, with an intuitive interface.
Additional features
- 1. Configurable web interface
- Customize the look and feel of the platform.
- 2. eConsent form with signature
- Obtain electronic consent directly within the system.
- 3. Image-based data entry
- Capture data from images.
- 4. Advanced validation rules and edit checks
- Ensure data accuracy and completeness.
- 5. E2B for pharmacovigilance
- Supports reporting of adverse events.
- 6. Upload & download files
- Manage study documents within the system.
- 7. Skip patterns (visible or enabled)
- Create dynamic forms that adapt to user responses.
- 8. Drop down list filtering & searchable lists
- Facilitate data selection and navigation.
- 9. Table designs (static and dynamic)
- Create and manage data tables.
- 10. Registry designs with higher-level grouping events
- Structure complex registry data.
- 11. eDiary capabilities (daily or hourly)
- Collect patient-reported data at regular intervals.
- 12. Visit scheduler email and phone reminder tracking
- Automate appointment reminders via SMS and email.
- 13. Secure fields to authorized users only
- Restrict access to sensitive data.
- 14. Full audit trail
- Track all data changes and user actions for compliance.
- 15. Automated text (SMS) reminders
- Send automated reminders to participants.
- 16. Electronic CRF (Case Report Form)
- Design and manage electronic case report forms.
- 17. Enrollment and randomization procedures
- Manage participant enrollment and randomization.
- 18. Participant surveys
- Conduct surveys within the platform.
- 19. Longitudinal study support
- Integrate various study components over time.
Pricing
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About Dacima Clinical Suite
Dacima Clinical Suite is a clinical data management software from Dacima Software that supports the management of clinical trials and research studies. It includes data collection tools, real-time reporting, and regulatory compliance features so researchers can efficiently manage their clinical data. The suite is designed to facilitate electronic data capture (EDC) and offers user-friendly interfaces for data entry and monitoring. Key capabilities: data collection real-time reporting regulatory compliance user interface customization multi-site management Best for: clinical researchers and trial managers that need a comprehensive solution for managing clinical trial data.
Dacima Clinical Suite Details
Dacima Clinical Suite's In-App Market Place
Does Dacima Clinical Suite have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
N/A
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), JPY (¥), CAD ($), AUD ($), CHF (CHF), CNY (¥), SEK (kr), INR (₹), SGD ($), HKD ($)
Pros & Cons
- • Affordable: Offers a cost-effective solution, especially compared to other custom EDC options.
- • User-Friendly: The interface is intuitive and easy to use, even for beginners.
- • Customizable: Highly flexible, allowing for tailored eCRF design and study-specific functionalities.
- • Excellent Support: Provides responsive and helpful customer support, often involving the CEO directly.
- • Comprehensive: Integrates various study components, including eCRFs, randomization, ePRO, and reporting, into one system.
- • Compliant: Fully compliant with regulatory requirements like Title 21 CFR Part 11.
- • Requires Support for Some Changes: Users may need technical support for certain complex modifications, although response times are quick.
- • Minor Interface Quirk: Saved changes on forms can cause the page to jump to the top, disrupting workflow slightly.
Dacima Clinical Suite's Support Options
Contact
+1 (514) 656-9199Dacima Clinical Suite's Alternatives
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