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
Suitable for a wide range of study types, including randomized clinical trials, observational studies, registries, eCOA/ePRO, and more.
Web interface, forms, and workflows can be tailored to specific study needs.
Includes electronic consent forms with signature capture.
Features robust data validation rules and edit checks.
Supports daily or hourly patient diary entries.
Meets industry standards, including FDA guidance and E2B for pharmacovigilance.
Cost-effective solution, even for academic budgets.
Responsive customer service and technical support, with expertise in clinical trial needs.
Easy to learn and use, with an intuitive interface.
Additional features
Customize the look and feel of the platform.
Obtain electronic consent directly within the system.
Capture data from images.
Ensure data accuracy and completeness.
Supports reporting of adverse events.
Manage study documents within the system.
Create dynamic forms that adapt to user responses.
Facilitate data selection and navigation.
Create and manage data tables.
Structure complex registry data.
Collect patient-reported data at regular intervals.
Automate appointment reminders via SMS and email.
Restrict access to sensitive data.
Track all data changes and user actions for compliance.
Send automated reminders to participants.
Design and manage electronic case report forms.
Manage participant enrollment and randomization.
Conduct surveys within the platform.
Integrate various study components over time.
Pricing
Countries & Languages
Interface languages
Billing currencies
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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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