THREAD named leader in the DCT Products PEAK Matrix® Assessment & winner of the Frost and Sullivan's “Customer Value Leadership Award” in the DCT industry.
The most complex eCOA on its own is not enough. The new generation of eCOA requires more features with less complexity versus the legacy platforms that fall short in both of these areas. #ClinicalResearch#DigitalHealth
Our own Noah Goodson, Ph.D. is working hard with our clients to focus on human-centered design to enhance the research study experience for patients and researchers around the globe. #ClinicalResearch#ClinicalTrial#DigitalHealth
Thank you Adam Kleger for your focus on enabling co-creation of protocols, schedule of events, informed consent language, patient recruitment materials and retention strategies with patients (and healthcare professionals). #ClinicalResearch#ClinicalTrial#DigitalHealth
Thank you Elizabeth Baldys for your focus on enabling co-creation of protocols, schedule of events, informed consent language, patient recruitment materials and retention strategies with patients (and healthcare professionals). #ClinicalResearch#ClinicalTrial#DigitalHealth
If you want to incorporate RWE data from Datavant in your Phase II trial, Phase IIIb/IV study or registry, our technology solution is something to see live. DM for more information or to schedule a session with our experts.#ClinicalResearch#ClinicalTrial#DigitalHealth
Explore "What Biology Can Teach Us about Patient-Centric Research". Discover how developmental biology principles intersect with clinical trial patient-centricity efforts, propelling a new era of research insights and strategies.
Learn more: https://t.co/J3hN8hXXcB
Discover deeper insights with inVibe's AI Multi-Project Chat, tailored for diverse projects. Learn how this feature is transforming the evaluation of cross-study data. Check out the complete article for further details: https://t.co/qi7SEAkxhc.
#MarketInsights#AIChat
Congratulations to Stephen Ryan, the Executive Director of Product, on being named a Top 100 Data and Analytics Professional at the 2025 OnCon Icon Awards! Stephen's dedication and proficiency continue to go above and beyond, and we're thrilled to acknowledge this recognition.
Interested in how electronic consent is changing the informed consent process? This piece explores the significance of digital signatures in participant interaction with consent documents.
Read the article: https://t.co/7qElxnikUx
Or request a demo: https://t.co/Ni19hbDJ51
As the clinical research moves towards digital solutions, eSource minimizes reliance on paper, optimizing data collection and administration, which boosts the quality and speed of research. Read more about the impact of eSource on the industry: https://t.co/wMMtfyyz8c
Discover the power of customizable insights with our new Configurable Reporting feature. Tailor your reports to fit your unique needs, streamline your data analysis, and make more informed decisions with ease.
Learn more: https://t.co/7ettiR0m99
Unlocking Clinical Trial Efficiency: Dive into "The Friction Factor". Learn how multi-stakeholder dynamics impact research processes and discover strategies to reduce friction for smoother trials.
#ClinicalResearch#TrialEfficiency
Read more: https://t.co/rTuZygmwsJ
Great to see this proposal being put forward, as Decentralized Clinical Trials (DCTs) offer an optimal solution for scenarios requiring accelerated approval.
Listen to Noah Goodson, on the role of Human-Centered Design principles in clinical trials. Analyzing data from over 250 global trials, Noah explores human-centered design to enhance patient experiences and outcomes.
View the webinar: https://t.co/O0Tr5YISDi
April is Parkinson's Awareness Month, highlighting the need to support those with the disease. This condition affects movement and mental health, making daily life challenging. Listening to patients helps us understand what frustrations they are facing. Listen to this clip.
Explore how to enhance patient engagement in clinical research through methods of co-creation and human-centered design. This helps align studies with participants' needs, leading to more effective and inclusive studies.
Read the full article here: https://t.co/KvY0Hq5haL
Curious how platform audit trails could help you identify potential data challenges in your study?
THREAD's Jennifer Price provides insight via a white paper published jointly by SCDM and eCLINICAL Forum: https://t.co/uUe8QJJLcb #ClinicalTrial#ClinicalResearch#DigitalHealth
Excited to announce the expansion of our Patient Voice Insight capabilities through the integration of generative AI, via Amazon Bedrock. This enhances the quality of automated insights gathered from patients.
Read the release: https://t.co/7avnqxLQn2
@invibelabs@AWS_Partners
We're looking forward to #PatientsAsPartners2025 next week. If you're attending, stop by booth #24, to learn more about our Patient Listening solution. Discover how our innovative method of gathering patient feedback, powered by generative AI insights, can enhance your studies.
Study timelines in clinical research are complex due to factors like screenshots, localized content & IRB submission timing. Reliance on eCOA vendors leads to risks & delays. Regulatory shifts offer opportunity to streamline processes & reduce dependencies https://t.co/93GtEz5GDN