NAMSA’s Post

ACDIS members save $150! The Clinical Validation in CDI Boot Camp training https://hubs.la/Q02Gcjmp0 enhances clinical indicators and collaboration with providers for CDI, aiming to improve expertise, critical thinking, & move towards genuine collaboration instead of just querying.

Join our experts, Jose Guethon MD, CDIP, and Jean Delva, RHIT, CDIP, CCS, CCS-P, at the HCCA Clinical Practice Compliance Conference on October 16th, 10:15 AM - 11:15 AM! Session 701: How to Measure Clinical Documentation Improvement Effectiveness & Maintain Provider's Engagement Level: Intermediate This session will offer valuable strategies for maximizing your CDI program and ensuring provider collaboration. You'll learn: • Metrics that healthcare organizations of all sizes can use to measure the effectiveness of clinical documentation improvement programs • Steps to gain a medical provider's buy-in in a clinical documentation improvement program (CDI) • Measures the organization can take to ensure queries in the CDI program are well-written and, most importantly, compliant Learn more here: https://lnkd.in/eZUWnKb4 #medicalcoding #HCCA #CDI #clinicaldocumentation #providerengagement #SymbionCoding

𝗜𝗳 𝘆𝗼𝘂 𝗵𝗮𝘃𝗲 𝗺𝗶𝘀𝘀𝗲𝗱 𝗼𝘂𝗿 𝗺𝗮𝘀𝘁𝗲𝗿𝗰𝗹𝗮𝘀𝘀 𝗼𝗻 𝗠𝗗𝗦𝗪/𝗦𝗮𝗠𝗗 𝘆𝗼𝘂 𝗰𝗮𝗻 𝘄𝗮𝘁𝗰𝗵 𝗶𝘁 𝗼𝗻𝗹𝗶𝗻𝗲! Many developers of MDSW/SaMD focus on technical aspects, overlooking elements that are crucial for certification. Clinical reviewers, on the other hand, evaluate your software from a healthcare professional's perspective. Join our masterclass to learn how to think like they do. Here the link: https://lnkd.in/eXA-_qXf #MDR #IVDR #MDSW #SaMD

Based on real-world clinical decision support (CDS) implementations, the AHRQ Clinical Decision Support Innovation Collaborative (CDSiC)'s newest resource provides a framework for analyzing reasons why recipients of #patient-centered clinical decision support (PC CDS) may choose not to follow the guidance. The Taxonomy of Override Reasons for PC CDS Recommendations can be used to better understand what can be done to improve PC CDS. https://lnkd.in/eNdb53Dq

Based on real-world clinical decision support (CDS) implementations, the AHRQ Clinical Decision Support Innovation Collaborative (CDSiC)'s newest resource provides a framework for analyzing reasons why recipients of #patient-centered clinical decision support (PC CDS) may choose not to follow the guidance. The Taxonomy of Override Reasons for PC CDS Recommendations can be used to better understand what can be done to improve PC CDS. https://lnkd.in/eNdb53Dq

VCT has cross-sponsor capabilities to detect duplicate research participants & "professional participants" within clinical trials and our ability to prevent this from happening at screening.    Detection of "professional" & duplicate participants is a key driver of RBQM activities. Detection is beneficial but by that time, it's too late. The participant has been enrolled, dosed, must be dropped, re-recruited, etc. It's a significant waste of time & money and risk to patient safety & data quality.   Our value is in our ability to prevent duplicate/professional participants from enrolling into a study by implementing the safeguards (VCT) at screening, thus enhancing data quality, integrity, and patient safety. The protections continue the entire duration of the study. #verifiedclincialtrials #professionalsubjects

Check out this new resource

Based on real-world clinical decision support (CDS) implementations, the AHRQ Clinical Decision Support Innovation Collaborative (CDSiC)'s newest resource provides a framework for analyzing reasons why recipients of #patient-centered clinical decision support (PC CDS) may choose not to follow the guidance. The Taxonomy of Override Reasons for PC CDS Recommendations can be used to better understand what can be done to improve PC CDS. https://lnkd.in/eNdb53Dq

🌟 Transforming Clinical Trials with AQ eISF 🌟 In the fast-paced world of clinical trials, being organised is not just an advantage, it's a necessity. At AQ Trials, we understand the critical need for efficiency, compliance, and speed in clinical trial documentation. Our innovative AQ eISF solution is designed to meet these needs seamlessly. Here are key features of AQ eISF that are revolutionising the way clinical trials are conducted: Digital Signature and Approval Workflows 📜✅ Streamline approvals and ensure compliance with secure, traceable digital signatures. Real-time Data Access and Collaboration 🌐🤝 Enhance collaboration and decision-making with real-time access to trial data from anywhere. Fully Enhanced Security and Compliance 🔒🛡️ Protect sensitive information with robust security measures and stay compliant with regulatory requirements. Integration with other Clinical Trial Systems 🔄🔗 Seamlessly connect with other systems used in your trials for a more cohesive and efficient workflow. By implementing these innovations, AQ eISF empowers your clinical trials to achieve faster completion times and improved outcomes. Let’s drive progress in clinical research together! 🚀 #ClinicalTrials #eISF #DigitalTransformation #HealthcareInnovation #ClinicalResearch #Efficiency #Compliance #AQTrial #DMS #Governance

Heading to the IHI Patient Safety Congress in May? Connect with our team (Booth 504) and discover how Pharmapod can drive efficiencies and enhance medication safety in your pharmacy. Key features: 👉 Incident Management: Access key insights into patient risks and real-time data with one click. 👉 Patient Safety Organization (PSO): Focus on quality improvement work in a safe, legally-protected environment. 👉 Assessments and Reports for Compliance: Conduct assessments, create action plans, follow up on measurements and activities, track important dates, view completion status, and store historical documents. 👉 Insights Pro/Analytics: Business intelligence tool for CQI, featuring comprehensive data analytics solution with 56 individual reports and exporting capabilities. 👉 Standard Operating Procedures/Document Management: Secure, digital document management to simplify pharmacy practice, communications and task completion. Learn more and schedule a meeting here: https://ow.ly/VOHu50R3xmW #PatientSafety #MedicationSafety #PSO #MedicationErrors #PharmacySafety #IHI #IHICongress