Signant Health (@signanthealth) 's Twitter Profile
Signant Health

@signanthealth

Signant is the evidence generation company. Our SmartSignals suite combines software with deep scientific expertise to deliver high quality #clinicaltrial data

ID: 1126887147758333952

linkhttp://www.signanthealth.com calendar_today10-05-2019 16:30:07

1,1K Tweet

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With our novel patient-reported outcome measure, PROMIS CAT, study teams can capture precise data from fewer questions or items, reducing completion burden for patients. Bonus: Incorporate it alongside traditional COAs. Get details: hubs.li/Q03pHd0z0

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The placebo effect is a contributing factor in the low success rates of novel pain medication #clinicaltrials, where less than 5% of low-abuse potential drugs gain approval. See how we helped one pharma company limit placebo effect and gain FDA approval: hubs.li/Q03pXfwG0

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Sites using too many systems? Our EDC offers add-on modules for eCOA, eConsent, and Randomization. One platform, one login, and happy sites. Take a look: hubs.li/Q03p_C9P0

Sites using too many systems? Our EDC offers add-on modules for eCOA, eConsent, and Randomization. One platform, one login, and happy sites. Take a look: 
hubs.li/Q03p_C9P0
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Leading technology without limits: Global pharmaceutical leaders rely on our comprehensive #eCOA, eClinRO, and #RTSM solutions for reliable evidence generation. No surprises, just flexible tech backed by expert teams. Explore industry-standard solutions: hubs.li/Q03qqH4H0

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Accelerate your vaccine research with trial-tested eCOA, RTSM, eConsent, telemedicine, and patient Engagement solutions. With experience in 200+ studies across 30+ countries, we're ready to help bring your vaccine to the public quickly and efficiently. hubs.li/Q03qFDSp0

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Pediatric depression #clinicaltrials have challenges: limited sites, variable CDRS-R administration, and complex multi-stakeholder interviews. See how our CDRS-R solution addresses them: hubs.li/Q03qS4BM0 #pediatricdepression

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How might placebo response and expectation bias impact #clinicaltrial outcomes? How can they be mitigated to ensure data reliability? Get answers from experts here: hubs.li/Q03rrgfB0

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🚀 Our TrialMax® platform features automation for the Data Change Form (DCF) process, reducing manual efforts, minimizing errors, and speeding up data management. Learn how TrialMax® is revolutionizing #eCOA study delivery: hubs.li/Q03rHZXD0

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Early detection of cognitive effects can make or break your clinical program. Our CDR system's attention battery identifies cognitive changes in early-phase #clinicaltrials, helping you make confident decisions before costly failures hubs.li/Q03rT4T40

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The therapeutic promise of #psychedelic compounds is real, but so are the scientific challenges. Our latest blog reveals evidence-based strategies to maintain methodological rigor and study integrity in psychedelic #clinicaltrials: hubs.li/Q03sfmDD0

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Our new "Getting Started with eCOA" series is your go-to resource for mastering the essentials of electronic COAs. Explore our quick-read guides and get the insights you need to succeed. Check it out now: hubs.li/Q03sHcfP0 #ClinicalTrials #eCOA #PatientCentricity

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Running GLP-1 RA trials? Our ePRO handles the complexities – from dose escalation tracking and cardiovascular assessments to participant retention. Streamline your data capture and engagement strategy: hubs.li/Q03tmgyq0

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How can PRO data help inform optimal dose selection in early-phase #oncology #clinicaltrials? Our new guide makes the case for incorporating patient experience data for a more complete tolerability assessment. Get it here: hubs.li/Q03tyk9c0

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When choosing an eClinical partner, biotechs and emerging biopharma shouldn’t have to choose between working with an established, full-service company and a provider with a hands-on approach. Get the best of both worlds: hubs.li/Q03tQxvT0

When choosing an eClinical partner, biotechs and emerging biopharma shouldn’t have to choose between working with an established, full-service company and a provider with a hands-on approach. Get the best of both worlds: hubs.li/Q03tQxvT0
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Signant's ops team has been recognized as a finalist for the OnCon Icon Top 100 Operations Team award. This recognition underscores our commitment to operational excellence as a catalyst for clinical research. Support innovation by voting for us: hubs.li/Q03vtr6S0

Signant's ops team has been recognized as a finalist for the OnCon Icon Top 100 Operations Team award. This recognition underscores our commitment to operational excellence as a catalyst for clinical research. Support innovation by voting for us: hubs.li/Q03vtr6S0
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Alzheimer’s trials are a maze. Let’s untangle the complexity together. Visit booth 1334 to talk with our team about optimal study design, reducing rater variability, ensuring eligibility, & building more signal-rich dementia trials. See details + posters: hubs.li/Q03vCXg30

Alzheimer’s trials are a maze. Let’s untangle the complexity together. Visit booth 1334 to talk with our team about optimal study design, reducing rater variability, ensuring eligibility, & building more signal-rich dementia trials. See details + posters:
hubs.li/Q03vCXg30
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Supply shortages derail study timelines and inflate budgets. Our Forecasting & Planning solution enables effective planning to prevent stockouts with real-time usage data and predictive modeling across your entire supply chain.  Protect study timelines: hubs.li/Q03vMzHq0

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Complex designs such as adaptive basket or umbrella trials are making RTSM builds more challenging. This blog covers best practices for implementation of adaptive trials: hubs.li/Q03wDz9n0 #RTSM #ClinicalTrials #AdaptiveTrials

Complex designs such as adaptive basket or umbrella trials are making RTSM builds more challenging. This blog covers best practices for implementation of adaptive trials: hubs.li/Q03wDz9n0 
#RTSM #ClinicalTrials #AdaptiveTrials
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At AAIC2025, our clinical science team will present data on screening optimization and endpoint reliability—two critical factors in successful Alzheimer’s disease trial design. Schedule time with our experts or get pre-conference resources: hubs.li/Q03xs13q0

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Subjective rating scales may challenge #immunology trials. The fix: electronic assessments with built-in standardization, specialized rater training, and real-time analytics. See this in a PsA trial: hubs.li/Q03xFQzr0 #ClinicalTrials

Subjective rating scales may challenge #immunology trials. The fix: electronic assessments with built-in standardization, specialized rater training, and real-time analytics. See this in a PsA trial: hubs.li/Q03xFQzr0
 #ClinicalTrials