Your Research CTMS
Your Research Clinical Trial Management System (CTMS) is tailored to streamline trials, prioritising patient-centricity and process efficiency. Key features ...
Why Choose Your Research CTMS?
Choose this if you want a clinical trial management system that’s all about making research smoother and more patient-friendly. It’s packed with automation and compliance features that really help keep trials on track.
Your Research Clinical Trial Management System (CTMS) is tailored to streamline trials, prioritising patient-centricity and process efficiency. Key features include protocol-driven automation for time-saving and accurate data input. Patient experiences are enhanced through digitalisation, optimising in-person tasks, visit bookings, and eConsent with a focus on improving retention. Predict future events by tracking historical metrics. Access user-friendly 'pay per play' eCOA modules, such as ePRO, eConsent, and eCRF, to elevate trial efficiency. Your Research CTMS is a comprehensive integrable solution, ensuring a seamless and patient-focused research experience. Your Research is compliant with and or adheres to the following best practices: - HIPAA - 21 CFR Part 11 - Good Clinical Practice (GCP) - ISO 27001 - GDPR - FDA 21 CFR Part 50 - FDA 21 CFR Part 54 - ICH E6 (R2)
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Your Research CTMS Introduction
What is Your Research CTMS?
Your Research is a leading Clinical Trial Management Software development company whose mission is to make a positive impact on people’s lives by advancing research processes that improve health outcomes. Your Research achieves this by offering the research industry a full suite of flexible, scalable, and integrable online modules derived from researcher led feedback. Your Research Clinical Trial Management System (CTMS) is tailored to streamline trials, prioritising patient-centricity and process efficiency. Key features include protocol-driven automation for time-saving and accurate data input. Patient experiences are enhanced through digitalisation, optimising in-person tasks, visit bookings, and eConsent with a focus on improving retention. Predict future events by tracking historical metrics. Access user-friendly 'pay per play' eCOA modules, such as ePRO, eConsent, and eCRF, to elevate trial efficiency. Your Research CTMS is a comprehensive integrable solution, ensuring a seamless and patient-focused research experience and is compliant with and or adheres to the following best practices: - HIPAA - 21 CFR Part 11 - Good Clinical Practice (GCP) - ISO 27001 - GDPR - FDA 21 CFR Part 50 - FDA 21 CFR Part 54 - ICH E6 (R2
How to use Your Research CTMS?
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Why Choose Your Research CTMS?
Choose this if you want a clinical trial management system that’s all about making research smoother and more patient-friendly. It’s packed with automation and compliance features that really help keep trials on track.
Your Research CTMS Features
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