RESOURCES & PERSPECTIVES
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Paper Vs ePRO: Clinical Data Collection Methods
7/16/2024
Patient-reported outcomes (PROs) assess patients' health without clinician interpretation. Traditional paper methods often result in missing data and quality issues, while electronic solutions enhance data accuracy and completeness.
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The Case For Cognitive Assessments In Phase 1 Clinical Trials
7/16/2024
Regulators prioritize patient-reported outcomes. Cognitive assessments in Phase 1 trials detect early drug-related cognitive effects, ensuring safety and efficacy. Signant’s CDR System® is a proven tool for this.
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Myasthenia Gravis: Reducing Outcome Measures Variability In Trials
7/16/2024
Myasthenia Gravis is a rare autoimmune disease often unknown to the public. This post explores MG's history, treatment progress, clinical trial challenges, and strategies to reduce outcome variability, improving patient care.
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Subjective Measures, Objective Outcomes: Data Quality In Atopic Dermatitis Trials
7/16/2024
Atopic Dermatitis (AD) is a prevalent skin condition. This post explores key measurement tools in AD clinical trials, specifically EASI and Total BSA, highlighting the importance of accurate measurement and strategies to improve data quality.
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Site Perspectives On BYOD ePRO Use
6/17/2024
This study examines participant convenience and compliance, aiming to understand and address the challenges faced by site personnel in global trials.
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How Site And Patient Research Optimizes Clinical Trials
6/17/2024
Signant’s patient and site research enhances digital health technology in clinical trials by optimizing usability and design. These insights drive improvements in product features, study designs, and training materials.
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Direct-To-Patient RTSM Solution
6/17/2024
Since the late 1990s, IRT has been central to clinical supply management. Modern decentralized trials now bring the supply chain into patient experience. This whitepaper explores direct-to-patient models and their pros and cons.
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eCOA Solution Design Recommendations: Applied Insights From Trial Sites, CRAs
6/17/2024
Enhance hybrid trials with digitalization through remote data capture using smartphones, tablets, and computers, improving participant experience and data integrity.
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Webinar Recap: How EDC Can Support Modern Clinical Trials
5/15/2024
Gain insights from our recent webinar focused on the critical role EDC systems play in supporting modern working practices and innovative trial designs, structured around four key themes.
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Navigating Audit Trail Data Regulations And Accessibility Changes
5/15/2024
Data is the single most important thing in a clinical trial. Leverage the power of clinical trial data with effective utilization and access in a changing regulatory landscape.