Castor

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)

Remember the annoying beeps of Palm Pilot eCOA devices? 🔔 Turns out, they were onto something. Simple, focused, and incredibly effective at driving compliance. Our latest blog delves into a recent conversation between Derk and eClinical Solutions Consultant Lisa Charlton, PhD, MBA, and asks, have we gone too far with modern eCOA complexity? 🤔 https://lnkd.in/eqNdafrK

🎬 CNS Summit said "make a fun video" Craig Lipset said "watch and learn" 👀🎙️ Derk said "hold my tea kettle" ☕️😆 Turns out filming yourself failing at outdoor survival is harder than it looks! But hey, we promise Derk's in-person chat game is stronger than his fire-starting skills 🔥 Send us a DM or book some time with Derk and the team in Boston here > https://lnkd.in/ecX5BHpK Jessica (Jess) Potestivo | Lewis C. B. | Solange M. | Daniella Mulder |