Castor

⎚ Think your trial docs are clear? Try them with 0.8% vision. 🤔 Joost Rigter did. Now, he's sharing his insights to help us make things better. Join Joost Rigter and Derk on December 11th, 10 am EST, to learn why accessible trial docs = better data. 📝 Bonus: AI's role in adaptive information 🤖

🚀 Self-serve clinical trials. 📱 BYOD by default. ⚡ API-first architecture. 🤖 AI-powered data entry. If these excite you, we're hiring: 🇳🇱 BENELUX Account Manager 🇺🇸 US Remote Solution Architect ✅ QA Validation Specialist 🌍 EMEA Sr Account Executive Learn more about these open positions, here → https://lnkd.in/eTBP9q_y

In clinical trials, imaging isn't just about taking pictures – it's about unlocking insights that can transform patient care. Here's 3 ways imaging drives research excellence: 🎯 Precision Patient Selection Enables researchers to build the right cohorts from day one 📊 Evidence That Speaks Volumes Captures disease progression with unprecedented clarity 🛡️ Guardian of Patient Safety Supports real-time monitoring for participant protection We've partnered with AG Mednet, Inc. to offer seamless imaging workflows that meet your trial's unique needs. Upload & de-identification of DICOM images, Endpoint adjudication, and more. Schedule a demo today to see how Castor simplifies image collection in clinical research > https://lnkd.in/eJZ6KP3K Dualtagh Franklin-Charlesworth, Sean Blank, Sarah Grady

🚰 The FDA's TAP program is transforming how AI-powered medical devices are brought to market. We're thrilled to see our friends at Ultromics secure their 6th FDA clearance for EchoGo Amyloidosis - a breakthrough in cardiac diagnostics. 🔬This signals a new era where regulators are actively creating pathways for innovative medical technologies. Smart regulation = faster innovation = better patient care. 💡 See how leading companies like Ultromics are leveraging modern data infrastructure to accelerate medical device development ➡️ https://lnkd.in/e-7KWNnz

Consent misconception: 'No signature required = no consent needed' Reality: 👍🏻 Waiver of Written Consent still demands full informed consent 👩🏽💻💬 Documentation can be digital/verbal 🤔 Participant understanding remains mandatory 📋 Process > Paperwork Are you confusing compliance with participant protection? Niecy Duncan, CCRC, PMP® breaks it down for you > https://lnkd.in/ejCc6yKP #ClinicalTrials #InformedConsent"

📊 The Numbers Tell a Story of Health Inequity: In South Dakota, 546 out of 649 syphilis cases were diagnosed in Native American communities - which represent just 9% of the state's population. This stark disparity raises critical questions: - How do we ensure our clinical research infrastructure reaches communities bearing the highest disease burden? 🦠 - What role does accessible research technology play in addressing health inequities? 👩🏽🔬 The answer lies in democratizing clinical research tools and empowering local healthcare providers with the right resources. 🔋👩🏽⚕️ That's where Castor for Impact comes in. Get *free access to the Castor platform if you’re running research on public health issues in underserved communities 🔗 https://lnkd.in/d-FbJpyS 🔗 #PublicHealth #HealthEquity #ClinicalResearch #HealthcareInnovation

Hey ISPOR Europe! 👋 Who's here? Our team is at booth 1420 chatting about powering RWE studies of all kinds and tackling complex data challenges. Look out for Amy Wright and Floris Morang! 👇👀 Dualtagh Franklin-Charlesworth is here somewhere too - deep in demo mode showcasing our modern, direct-to-patient technology. 💫 Stop by and meet the team, or learn more here: https://lnkd.in/eV8sGrf4 #ISPOREurope #RealWorldEvidence

📊 Hard truth: Missing ePRO data doesn't just create gaps - it undermines the entire premise of real-world evidence. At Castor, our >90% compliance rates aren't just numbers - they're proof that patients want to share their stories when given the right tools. 🎯 The FDA isn't suggesting PRO collection for RWE studies - they're demanding it. Why? Because without consistent patient voices, we're just guessing at outcomes that matter. ⚡️ Stop chasing participants for missed entries. Our compliance dashboard flags engagement drops before they become data integrity issues. Every missed entry is a missed opportunity to understand patient experiences. Schedule a demo today ➡️ https://lnkd.in/eJZ6KP3K #WorldQualityDay #WorldQualityWeek #Quality #QMS #MedTech Fatma Elfaghi, CQA, Tanu Agrawal, Christian Devonport-McGowan, Dualtagh Franklin-Charlesworth, Sébastien Bohn, Lisa Charlton, PhD, MBA

"Traditional quality control can delay trials. Quality culture accelerates them." 💡 Our quality leaders Fatma Elfaghi, CQA and Tanu Agrawal share the proof: 🔵 Test automation catches the majority of issues before production 🫴🏼 🔵 Continuous feedback loops drive faster, safer deployments ⚡ 🔵 4-8 week average study start-up time ⏰ 🔵 100% on-time study implementation record 💯 This #WorldQualityDay discover how quality-driven culture transforms clinical trials from compliance-focused to performance-driven, improving patient outcomes and research efficiency:  https://lnkd.in/euDNVRXw #WorldQualityDay #WorldQualityWeek #ClinicalTrials #HealthTech #Quality #QMS #MedTech

🤖 Can AI actually help with study design, or is it just another buzzword? Join Derk at #DTRA2024 where he'll challenge assumptions alongside Anindita (Annie) Saha from the FDA, AMIR KALALI, MD, @Melissa Ceroulo from Medidata and Craig Serra from Flatiron. 🎯 Nov 15, 9:25 AM 🤝 Book a meeting with Derk at DTRA here: https://lnkd.in/evFtk58q or DM #ClinicalTrials #AI #DecentralizedTrials Decentralized Trials & Research Alliance (DTRA)