Castor EDC by Castor
Castor EDC is an electronic data capture platform for clinical trials that helps research teams build studies, integrate data from multiple sources, and run decentralized trials wi...
secuTrial is a robust, web-based Electronic Data Capture (EDC) and clinical data management system designed for clinical trials of all phases and complexities. It is built with a strong emphasis on regulatory compliance, providing built-in features and audit trails that fully support adherence to Good Clinical Practice (GCP) guidelines and U.S. FDA 21 CFR Part 11 regulations for electronic records and signatures. The system offers comprehensive tools for building studies, capturing data, managing queries, and ensuring data integrity and security throughout the trial lifecycle. This solution is targeted at pharmaceutical and medical device companies, academic research organizations, and CROs conducting clinical trials that require a powerful, fully co...
This solution is targeted at pharmaceutical and medical device companies, academic research organizations, and CROs conducting clinical trials that require a powerful, fully compliant, and reliable EDC system to meet stringent international regulatory standards.
secuTrial is a heavyweight in the compliant EDC space. Its proven track record and built-in focus on GCP and Part 11 compliance make it a trusted and secure choice for sponsors conducting trials where regulatory scrutiny is high and data integrity is paramount.
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This solution is targeted at pharmaceutical and medical device companies, academic research organizations, and CROs conducting clinical trials that require a powerful, fully compliant, and reliable EDC system to meet stringent international regulatory standards.
These are common features buyers compare in Clinical Trial Management Software. Product-specific availability should be confirmed with the vendor.
Helps buyers evaluate how access, control, and evidence are handled for sensitive or regulated work.
Shows how well the product can connect with existing systems and reduce duplicate data entry.
Keeps important files and records close to the workflow, with easier search, review, and handoff between teams.
Helps buyers judge whether double data entry fits the way their team handles clinical trial management work.
Helps buyers judge whether electronic data capture fits the way their team handles clinical trial management work.
Helps buyers judge whether EMR or EHR fits the way their team handles clinical trial management work.
Connects money-related work with the rest of the clinical trial management process so charges, approvals, and records are easier to review.
Helps buyers judge whether HIPAA compliant fits the way their team handles clinical trial management work.
Tracks the items, locations, or resources the team depends on so availability and ownership are easier to confirm.
Keeps person or account details tied to the work they affect, instead of leaving context scattered across notes and inboxes.
Gives managers a clearer view of activity, exceptions, and trends so they can spot issues before they turn into rework.
Keeps person or account details tied to the work they affect, instead of leaving context scattered across notes and inboxes.
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