Patient Data Reporting Solutions
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Electronic Informed Consent For Clinical Research
2/16/2024
We partnered with leading academic medical centers, sponsors, hospital systems, and site networks to create an eConsent platform that is easy-to-use and minimizes risk.
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Your Early "Warning System" To Assess Risks To TMF Health
4/19/2022
Introducing the TMF Health Score – an expert methodology that provides an “early warning system” to commonly overlooked issues that often lead to inspection findings.
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Medidata eConsent – Empowering Patients Right From The Start
8/2/2021
Medidata’s eConsent is an innovative, patient-friendly, electronic informed consent and patient enrollment system for clinical trials. Through the use of multimedia technology, your patients are educated and guided through understanding key elements of a clinical trial.
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Assess And Optimize Ratings Reliability
8/30/2023
See how this centralized solution for clinical ratings enhances the precision and dependability of data obtained from assessments based on clinician-reported outcomes (ClinROs), thus achieving elevated data quality.
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Unified, Integrated eClinical Research Solutions
1/16/2024
Facilitate efficient digitalization and optimization of clinical trials that meet the unique needs of small and mid-size biopharma organizations with the Signant SmartSignals Unified Platform.
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Cut Study Start-Up Times By Up To 50% With eCOA
8/24/2023
Improve study start-up experiences with flexible deployment options, a groundbreaking global instrument library, and dedicated services and support offered by Medidata’s eCOA.
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Patient-Focused Clinical Development: Computerized Adaptive Tests
8/29/2023
Discover more about this eCOA innovation, PROMIS CAT, and its profound impact on augmenting PRO data quality while prioritizing patient-centricity in clinical development, by accessing the brochure below.
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Selecting And Evaluating An eRegulatory Solution
10/6/2023
Take advantage of this checklist for evaluating eRegulatory solutions for clinical trial offices.
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eSource Element
4/28/2022
As industry experts in DCT, MRN has delivered innovative solutions using our specialized expertise and creative approaches, providing in-home clinical trial visits through their Home Trial Support service to over 230 trials.
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Evaluating Cognitive Safety In Clinical Trials
2/21/2025
Understanding cognitive function is essential in drug development. Explore how you can utilize cognitive tests to evaluate treatment effects on cognition with unrivaled accuracy and sensitivity.