RxLogix Corporation

Save the Date, Mark your calendars! 🗓️✨Don’t miss this!

This webinar will demonstrate how PV Publisher can help you achieve up to 80% time savings with automation, streamline your regulatory submissions, and simplify the reporting process. Why You Should Attend: · Seamless integration with your existing PV systems. · Eliminate the inefficiencies of custom solutions for aggregate reporting. · Achieve faster and more accurate submissions for PV Agreements and PSMF files. Date & Time: 4th February 9:00 - 10:00 AM EST Register here: https://lnkd.in/efTnKuMz #pharmacovigilance #pvsystems #rxlogix #efficiency #webinar

RxLogix: No shenanigans, no gimmicks, no fluff—just results that speak volumes

From Strength to Strength: Celebrating 14 Years of Excellence On December 6, 2024, we proudly celebrated 14 years of innovation, resilience, and impact at RxLogix. From our humble beginnings to becoming a leader in pharmacovigilance, our journey has been nothing short of extraordinary. Here’s a glimpse of what makes this milestone special: • Innovation at Our Core: For over a decade, we’ve driven cutting-edge solutions, earning accolades like the 2020 Global Pharmacovigilance Automation Software Product Leadership Award and ranking #1 for Case Intake & Processing Automation. • Fast-Growing Success: RxLogix is among the top 3.5% of companies to make the Inc. 5000 list six times since 2018, a testament to our consistent growth and excellence. • Landmark Partnerships: Our recent collaborations with FDA and EMA underscore our commitment to shaping the future of patient safety through innovative solutions. Thank you to our dedicated team, loyal customers, and invaluable partners for making this journey possible. Together, we’re building a legacy of trust, progress, and global impact. Here’s to the next chapter of unparalleled success! #14YearsOfRxLogix #Innovation #Excellence #Pharmacovigilance #Partnerships #Growth

SIAB: Your plug-and-play solution for ultimate peace of mind. Interested? Inspired? Curious? Questions? Let’s talk-let us connect over a call or a cup of coffee-and we can show you some real-life case studies: Reach out to us at Info@rxlogix.com or Sales@rxlogix.com

This webinar will demonstrate how PV Publisher can help you achieve up to 80% time savings with automation, streamline your regulatory submissions, and simplify the reporting process. Why You Should Attend: · Seamless integration with your existing PV systems. · Eliminate the inefficiencies of custom solutions for aggregate reporting. · Achieve faster and more accurate submissions for PV Agreements and PSMF files. Date & Time: 4th February 9:00 - 10:00 AM EST Register here: https://lnkd.in/efTnKuMz #pharmacovigilance #pvsystems #rxlogix #efficiency #webinar

Combining Safety, Efficacy and Pharmacoeconomics Endpoints

Join our upcoming webinar to see how PV Publisher can deliver: • Seamless integration with your existing PV systems—get up and running quickly. • Effortless design to eliminate the inefficiencies of custom solutions for aggregate reporting and regulatory submissions. • Automation to simplify the creation and submission of PV Agreements, PSMF files, and aggregate reports, achieving up to 80% time savings. Date & Time: 4th February 9:00 - 10:00 AM EST Register here: https://lnkd.in/efTnKuMz #pharmacovigilance #pvsystems #rxlogix #efficiency #webinar

How RxLogix platform deals with Rare and Ultra Rare ADRs? By combining cutting-edge technology with a deep understanding of PV domain requirements, RxLogix ensures integrated, end-to-end management of rare and ultra-rare ADRs, helping pharma, biotech’s enhance patient safety & maintain regulatory compliance. -Advanced Signal Detection: RxLogix platform uses sophisticated AI/ ML algorithms to identify patterns in data that suggest a rare or ultra-rare ADR. This involves analyzing large datasets and doing data mining on/from various sources, including clinical trials, post-market surveillance, & spontaneous reporting systems. - Comprehensive Data Integration: RxLogix integrates data from diverse sources such as electronic health records (EHRs), medical literature, & regulatory databases. This integrated approach helps in capturing rare ADRs that might not be evident from a single data source. -Automated Processes: Tasks such as data entry, case processing, and signal detection are automated in RxLogix Platform. This not only speeds up the process but also reduces human error, ensuring that rare ADRs are detected & reported accurately. -End-to-End Solution: From data collection to risk assessment, RxLogix platform offers an integrated approach. This means that once a potential signal is detected, it can be further investigated & assessed within the same system, ensuring a seamless flow of information. -PV Quality Monitoring: The data quality of cases is critical, especially for rare ADRs. RxLogix platform includes tools to monitor & ensure the quality of data entered, which is crucial for accurate analysis & decision-making. -Rare Disease and Orphan Drug Support: RxLogix's platform supports the unique requirements of rare disease treatments, aligning with specific regulatory guidelines for orphan drugs. -Regulatory Reporting and Compliance: RxLogix platform ensures seamless compliance with requirements like FDA’s FAERS, EMA’s EudraVigilance, & other global safety databases tailored to rare ADRs. -Interactive & Unified Platform: Enables integration with global data-sharing initiatives, such as rare disease consortia, ensuring broader context & understanding of rare ADRs. Single source of truth for sponsors, CROs, and researchers to contribute to & access rare ADR findings. -Proactive Risk Mitigation: Predictive Analytics: Anticipates potential risks by analyzing historical & prospective data trends. Risk Management Plans (RMPs): Facilitates the creation and execution of tailored RMPs for drugs with a known risk of rare ADRs. -User-Friendly Dashboards: Interactive dashboards help siloed teams visualize & analyze trends in rare ADR reporting effectively. Want to see it in action, reach out to us at info@rxlogix.com

Join our upcoming webinar to see how PV Publisher can deliver: - Seamless integration with your existing PV systems—get up and running quickly. - Effortless design to eliminate the inefficiencies of custom solutions for aggregate reporting and regulatory submissions. - Automation to simplify the creation and submission of PV Agreements, PSMF files, and aggregate reports, achieving up to 80% time savings. Date & Time: 4th February 9:00 - 10:00 AM EST Register here: https://lnkd.in/efTnKuMz #pharmacovigilance #pvsystems #rxlogix #efficiency #webinar