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Whether you're further along the journey to IDMP readiness, or just about to start, our handy information sheet will help you learn all the essentials: Guidance from EMS's PMS Info Day, ISO IDMP Implementation, System Readiness, ESMP 2025 Preparation and more. We're here to help you navigate these changes with the CARA Life Sciences Platform providing: ▶ Seamless Connectivity: Managing the entire IDMP process ▶ Structured Information Lake: Data accessible across departments ▶ Flexible Templates: Covering various output cases ▶ Logical Data Management: Facilitating data governance ▶ EMA Alignment: Ensuring compliance with guidelines Read the full summary from our webinar here : https://lnkd.in/efktPPbm If you want to see more IDMP news, please let us know in the comments! #IDMP #Regulatory #EMA #Compliance #PMS #CARA #datamanagement  

We recently hosted a webinar 'Ontology-Drive Integration: IDMP Efforts with a Fair Outcome' with our partners MAIN5. If you missed it, don't worry! You can read our summary and see a short demo below. Learn how your business can benefit from the integration of IDMP with a focus on FAIR data principles, showcasing how ontology-driven approaches can ensure effective data interoperability in regulatory frameworks. Read more here : https://lnkd.in/eXrjQaCR #webinar #IDMP #datamanagement

🤔 How can you align your Data Workflows with Regulatory Standards and empower Investigators in decision-making? The answer is waiting for you in our #SCDM free industry webinar brought to you by Viedoc. We’ll hear Alan Yeomans and Sverre Bengtsson to walk us through the exclusive insights from on adapting workflows to align with regulatory demands. Join us on February 15 to discover the strategies and techniques how to leverage state-of-the-art #technologies for compliant #datamanagement. Register for free ➡️ https://lnkd.in/eQwJvPb2 #SCDMLearning

Setting a new course to innovate beyond the limitations you're facing in #regulatory functions within Life Sciences? Interested in shaping a better understanding of exactly how you can begin to define or even accelerate progress against, your digital transformation strategy? Then Join us in Cambridge for our Regulatory Transformation Forum! Connect with other Leaders & Innovators to discuss emerging capabilities & the methods to leverage them in achieving data-driven transformation across strategic imperatives around KASA, IDMP, FHIR standards, and dossier automation. Key Discussion Points Include: 🚀 Overcoming the most pressing data challenges to drive document automation, data-reuse, and enhanced accuracy and traceability in dossier authoring 🔥 Driving data automation & authoring efficiency while building a foundation for FHIR standards and Digital Exchange 📈 Increase confidence & progress against a variety of strategic, digital imperatives Send me a message for the details and a Registration Link to join us!

🔔Don't miss the webinar "ICH E6(R3) Essentials: A Draft Guidance Overview" happening February 6th!🔔 Hosted by Karen Harvey, Senior Director, Avoca Quality Consortium, and lead contributor of the just-released online resource "Tracking the Revised ICH E6: A Side-by-Side Comparison of Revisions 2 and 3."  This webinar will highlight changes to the ICH E6 guidance, including:  📝New and revised principles of good clinical practice  🩺Expanded oversight responsibilities for investigators  📊The new Data Governance section  ⭐⭐⭐And more!  See details and secure your spot at https://lnkd.in/dJGi9HPz Presented by CenterWatch, A WCG Company in collaboration with Avoca, A WCG Company #clinicalresearch #clinicaltrials #regulatoryguidance #ICHE6 #WCG  

Get a behind-the-scenes look at #pharmacyclaimsprocessing during our upcoming #webinar, The Story of a Claim, hosted by VP of Product Management Kevin Sundquist! 💡 Learn everything that goes into this complex process, how a modern platform can help streamline things, and: ⏰ How real-time processes influence the claim’s journey and reduce turnaround times ✅ Tools that allow for accurate records and thorough follow-up after a claim is paid ⚡️ The ways a #modern system provides transparency during the adjudication process (while simultaneously speeding it up) Register today and save your spot for the webinar! #healthtechinnovation #knowledgesharing #PharmacyBenefitAdministration https://okt.to/gxI3Ky

🧭 navigating the maze of early assets' future value 🧭 Clients and colleagues often ask me what is needed to plan for access and pricing success of early-stage assets (up to proof-of-concept clinical studies). We're lucky at Inbeeo that half of our projects are in support of early assets, including those that have been identified as targets for acquisition by our clients. Developing and curating a value framework that helps triangulate the value of an asset is one of the most cost-effective ways to support a due diligence. And i-vbp(r) is probably the best value framework tool available. Check out this case study and how we helped a midsize pharma client funnel down from 200 targets to one acquisition in rare CNS. https://lnkd.in/ej3kWwXw

As changes within the life sciences industry remains rampant, a pro-active, digital quality management approach is critical. In this fireside chat, IQVIA’s Michael King and Frost & Sullivan’s Sankara Narayanan discuss the five most important trends in the QMS market and why SmartSolve® is the most complete eQMS purpose built for life sciences. https://bit.ly/3OfMvvb #eQMS

🌟 Transform Indication Prioritization and BD&L Strategies with i-vbp®! 🚀 Quantitatively comparing the overall value of one asset against another can be complex, but with i-vbp®, we simplify the process. Our Inbeeo Value-Based Pricing (i-vbp®) framework puts the power of Multi-Criteria Decision Analysis (MCDA) in your hands, allowing you to capture the relevant value of your asset or indication for your key stakeholders. i-vbp® is an easy-to-use, secure, cloud-based application. We collaborate with you to customize a value framework that aligns with your specific needs. Your value framework is entirely transparent and can be dynamically modified to reflect different locations and stakeholder perspectives. Discover how i-vbp® empowered one of our clients to swiftly make decisions regarding indications and assets to pursue; or reach out to Herve Lilliu or Erin Haney for an i-vbp® demo! #lifesciences #marketaccess #ivbp #raredisease #drugpricing #hta #valuebasedpricing #mcda #MultiCriteriaDecisionMaking

The life sciences industry is on the cusp of a data revolution, with IDMP at its core. However, many organisations are grappling with the challenges of integrating SPOR services, aligning with FAIR principles, and leveraging ontologies effectively. We've teamed up with our partners MAIN5 to bring you a webinar covering all the key information. Register here : https://lnkd.in/e-Ri2ETB Let's turn data challenges into opportunities together! #IDMP #regulatory #datamanagement #ema #webinar