Dr. Chardae Rodgers-Gamble’s Post

Elevate Your Clinical Research Experience with CR Clinical! Unlock the potential of cutting-edge solutions and a digital-first approach to clinical research at buff.ly/35CKhQP. Discover our unified, cloud-based platform that optimizes trials for maximum efficiency, encompassing Patient Reported Data, Clinical Reported Data, CTMS, ePRO / eCOA / eTMF, EDC (eCRF), eConsent, Randomization/Product Assignment, and AE/SAE Reporting. Experience seamless data infrastructure and workflows ensuring compliance with 21CFR Part 11 standards, powered by our app-based platform (iOS/Android) for site-based, hybrid, and decentralized trials. Automate investigator & participant engagement, integrate lab and imaging results, and benefit from integrated validation/audits and redaction. Explore our professional clinical trial support services, from protocol development to regulatory guidance and statistical analysis. Ready to revolutionize your clinical research? Contact us today at 📧 info@crclinical.com or 📞 215-394-0048. #ClinicalResearch #CRClinical #DigitalCRO #OptimizedTrials #ResearchInnovation

📊 Unlock the Future of Clinical Research with Our Digital-First CRO Experience! 🌐 Discover the power of a unified, cloud-based platform that delivers all major clinical systems, streamlining your trials for optimal efficiency, including Patient Reported Data, Clinical Reported Data, CTMS, ePRO / eCOA / eTMF, EDC (eCRF), eConsent, Randomization/Product Assignment, and AE/SAE Reporting. Experience a seamless data infrastructure and workflows, ensuring compliance with 21CFR Part 11 standards, with an app-based platform (iOS/android) that powers site-based, hybrid, and decentralized trials, automates investigator & participant engagement, and integrates lab and imaging results. Realize the benefits of integrated validation/audits and redaction. Plus, explore a range of professional clinical trial support services, from protocol development to regulatory guidance and statistical analysis. Ready to revolutionize your clinical research? Contact us today at 📧 info@crclinical.com or 📞 215-394-0048. #ClinicalResearch #CRClinical #DigitalCRO #ClinicalTrials #OptimizedDataInfrastructure #ResearchInnovation

📊 Unlock the Future of Clinical Research with Our Digital-First CRO Experience! 🌐 Discover the power of a unified, cloud-based platform that delivers all major clinical systems, streamlining your trials for optimal efficiency, including Patient Reported Data, Clinical Reported Data, CTMS, ePRO / eCOA / eTMF, EDC (eCRF), eConsent, Randomization/Product Assignment, and AE/SAE Reporting. Experience a seamless data infrastructure and workflows, ensuring compliance with 21CFR Part 11 standards, with an app-based platform (iOS/android) that powers site-based, hybrid, and decentralized trials, automates investigator & participant engagement, and integrates lab and imaging results. Realize the benefits of integrated validation/audits and redaction. Plus, explore a range of professional clinical trial support services, from protocol development to regulatory guidance and statistical analysis. Ready to revolutionize your clinical research? Contact us today at 📧 info@crclinical.com or 📞 215-394-0048. #ClinicalResearch #CRClinical #DigitalCRO #ClinicalTrials #OptimizedDataInfrastructure #ResearchInnovation

📊 Unlock the Future of Clinical Research with Our Digital-First CRO Experience! 🌐 Discover the power of a unified, cloud-based platform that delivers all major clinical systems, streamlining your trials for optimal efficiency: ✅ Patient Reported Data and Events ✅ Clinical Reported Data, Images, and Events ✅ CTMS ✅ ePRO / eCOA / eTMF ✅ EDC (eCRF) ✅ eConsent ✅ Randomization/Product Assignment ✅ AE/SAE Reporting Experience a seamless data infrastructure and workflows, ensuring compliance with 21CFR Part 11 standards: 📱 App-based platform (iOS/android) 💡 Powering site-based, hybrid, and decentralized trials 🤖 Automate investigator & participant engagement ✍️ eConsent, medical history, I/E, ePRO, eCOA 🚀 Automate CRF, protocols, alerts, and reminders 🧪 Lab and Imaging result integration and visibility 📊 Real-Time AE/SAE reporting and categorization 🔍 Integrated validation/audits and redaction Plus, we offer a wide range of professional clinical trial support services, from protocol development to regulatory guidance and statistical analysis. Ready to revolutionize your clinical research? Contact us today for tailored solutions that fit your needs at: 📧 info@crclinical.com 📞 215-394-0048 #ClinicalResearch #CRClinical #DigitalCRO #ClinicalTrials #OptimizedDataInfrastructure #ResearchInnovation

📊 Unlock the Future of Clinical Research with Our Digital-First CRO Experience! 🌐 Discover the power of a unified, cloud-based platform that delivers all major clinical systems, streamlining your trials for optimal efficiency: ✅ Patient Reported Data and Events ✅ Clinical Reported Data, Images, and Events ✅ CTMS ✅ ePRO / eCOA / eTMF ✅ EDC (eCRF) ✅ eConsent ✅ Randomization/Product Assignment ✅ AE/SAE Reporting Experience a seamless data infrastructure and workflows, ensuring compliance with 21CFR Part 11 standards: 📱 App-based platform (iOS/android) 💡 Powering site-based, hybrid, and decentralized trials 🤖 Automate investigator & participant engagement ✍️ eConsent, medical history, I/E, ePRO, eCOA 🚀 Automate CRF, protocols, alerts, and reminders 🧪 Lab and Imaging result integration and visibility 📊 Real-Time AE/SAE reporting and categorization 🔍 Integrated validation/audits and redaction Plus, we offer a wide range of professional clinical trial support services, from protocol development to regulatory guidance and statistical analysis. Ready to revolutionize your clinical research? Contact us today for tailored solutions that fit your needs at: 📧 info@crclinical.com 📞 215-394-0048 #ClinicalResearch #CRClinical #DigitalCRO #ClinicalTrials #OptimizedDataInfrastructure #ResearchInnovation

Prepare to streamline data management and automate data capture with dynamic, comprehensive eCRFs, taking your clinical trials to a whole new level. Our EDC platform lets you build, capture, and report on your clinical data with ease. See it in action in a free demo today: https://bit.ly/3MKyFQn #ClinicalResearch #EDC #ClinicalTrials

🌟 We are NOT fooling around with our next webinar! The next installment of the Galen Data Medical Device Innovation webinar series will be on Tuesday, April 23 at 12pm CT. In this edition, we will be joined by Chris Rush from Greenlight Guru in "Challenges of Clinical Data Collection in MedTech, and Why It's Worth It" where we will discuss regulatory requirements for clinical data collection for varying device classes, the challenges associated therein, and best practices for successfully planning and delegating the duties involved in running a study. We will discuss how to engage with partners, software vendors, and provide an answer to the question: “Is this all worth it?” What can you expect to learn? ✔ Why collecting data for Class II and Class III devices is valuable ✔ Timeline/cost challenges for running clinical studies ✔ How to efficiently plan and delegate activities for data collection, including CRO and EDC software selection Learn more and register here: https://lnkd.in/gen3jWnM

🌟 TX Medical Leads with CDISC-Compliant Clinical Research for Medical Devices 🌟 We're proud to announce a significant milestone in our journey towards enhancing medical device innovation and regulatory compliance. At TX Medical, all our medical device clinical research projects now strictly adhere to the Clinical Data Interchange Standards Consortium (CDISC) requirements. This includes the establishment of Electronic Data Capture (EDC) systems, meticulous data management, and rigorous statistical analysis, ensuring full compliance with the regulations set by China's National Medical Products Administration (NMPA). This initiative aligns with the NMPA's directive (No. 121 of 2021) mandating the submission of a clinical trial database for medical devices undergoing clinical evaluation through clinical trials for registration applications. Our adherence to CDISC standards not only streamlines the registration process but also significantly enhances the integrity and reliability of clinical trial data. At TX Medical, we're committed to setting the standard for excellence in medical device clinical research. Our dedication to regulatory compliance and data standardization positions us at the forefront of medical device innovation, ensuring that we continue to meet the evolving needs of patients and healthcare professionals worldwide. For more insights into our clinical research services and our approach to meeting regulatory standards, reach out to us at contact@txmedical.com. #MedicalDeviceInnovation #ClinicalTrials #DataStandardization #RegulatoryCompliance #TXMedical #HealthcareInnovation

🌐 A Milestone Achievement for TX Medical 🌐 As the founder of TX Medical, I am thrilled to share a pivotal advancement in our commitment to revolutionizing the medical device industry. Starting February 1, 2024, every clinical research project under our umbrella rigorously adheres to the Clinical Data Interchange Standards Consortium (CDISC) requirements. This includes the comprehensive implementation of Electronic Data Capture (EDC) systems, alongside precise data management and statistical analysis, in strict compliance with the regulations set forth by China's National Medical Products Administration (NMPA). This strategic move is not just about adhering to the NMPA's directive (No. 121 of 2021) that mandates the submission of clinical trial databases for medical devices. It's about setting a new standard in the industry. Our dedication to utilizing CDISC standards streamlines the registration process, bolsters the integrity and reliability of clinical trial data, and, most importantly, accelerates the delivery of innovative medical devices to those who need them most. At TX Medical, we are not just conducting clinical research; we are pioneering a path for future medical device innovation and regulatory compliance. Our commitment to excellence and regulatory adherence is a testament to our dedication to improving patient care and healthcare outcomes worldwide. I invite our partners, clients, and the broader healthcare community to join us in this exciting journey. Together, we can drive the future of healthcare innovation. For more information on our clinical research services and our approach to regulatory standards, please feel free to connect with me via contact@txcro.com #MedicalDeviceInnovation #ClinicalTrials #DataStandardization #RegulatoryCompliance #TXMedical #HealthcareInnovation

Clinical trial technologies are not just for data collection. Read about how our Clinical Operations team uses technology to help with trial management. https://lnkd.in/e2uizV8Y