Generis’ Post

Join MAIN5 and our partner Generis for an insightful webinar on "Ontology-Driven Integration: IDMP Efforts with a FAIR Outcome," where we'll unlock the secrets to seamless data integration and IDMP compliance. 🗓 Spt.17, 2024 🕒 2pm BST I 3pm CEST I 8am CDT I 9am EDT 🌐 Register Here: https://lnkd.in/d7zYNYUK The webinar is designed to provide a comprehensive understanding of how ontology-driven methods can lead to a FAIR outcome in IDMP data integration, setting a new standard for data management in the industry. We will provide invaluable insights into: 🔸 The pivotal role of SPOR services within the EMA’s master data management strategy 🔸 How integrating these services with key applications is revolutionising data quality and availability, significantly reducing manual labour and rework 🔸 The power of IDMP ontology (IDMP-O) and knowledge graphs for achieving true data interoperability 🔸 Aligning master data management with FAIR principles to ensure your data is Findable, Accessible, Interoperable, and Reusable 💻 Secure your spot today and be part of the conversation that shapes the future of data interoperability. Register here: https://lnkd.in/d7zYNYUK #IDMP #IDMPOntology #FAIRdata #LifeSciences #DataManagement #Webinar #EMA #MasterDataManagement

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  

In case you missed the webinar "PMS and IDMP: Latest Guidance and What You Need to Do to Prepare" organized by Generis, here are some highlights and key insights 👇 Remco Munnik provided an in-depth overview of the current IDMP landscape and the latest updates from the PMS Info Day. Jack Kelleher demonstrated Generis' innovative data management platform designed to guide organizations towards IDMP readiness. 🙏 A big thank you to Karolina Rogowska and the Generis team for organizing this informative webinar! #Iperion #aDeloittebusiness #IDMP #PMS #DataManagement

Data transfer security is a challenge We will listen to you Sibel

Aggregating your PK data is the first step in any pharmacometric workflow. Integral, the data repository component of Certara’s Phoenix Platform, lets global teams like Charles River Laboratories do just that. See how in our on demand webinar: https://ow.ly/HbjX50Sr7Ls

#ScispotImpact: 95% Accuracy & 70% Fewer Errors for faster, high-quality diagnostics 🧬📊 A Canada-based molecular diagnostics lab struggled with fragmented data, manual errors, and integration challenges. Scispot alt-SDMS helped improve data quality, automate processes, and enhance regulatory compliance. Here’s how Scispot made a difference: 👉 Challenge: Inconsistent data quality, manual errors, and integration gaps. 👉 Solution: Scispot automated data integration, real-time validation, and audit-ready documentation. 👉 Impact: 95% improved accuracy, 70% fewer data entry mistakes, and faster, high-quality diagnostics. ✨ Discover how Scispot helps labs: scispot.com/demo

Data Transfer Specifications (DTS) are crucial for ensuring seamless integration of non-CRF data in clinical trials. In her latest blog, Erin Erginer, Senior Director of Product at Certara, highlights the importance of establishing clear DTS guidelines to maintain data integrity and accelerate submission timelines. Discover how a robust DTS framework can improve vendor collaboration and enhance trial outcomes: https://ow.ly/Uy1p50Tx7Wi #Certara #ClinicalResearch #ClinicalTrials #DataManagement #NonCRFData #DrugDevelopment

October Webinars on SPOR and xEVMPD during which EMA’s SPOR team will cover all aspects of regulatory data management and the way SPOR and xEVMPD work today. Use this opportunity. The sessions will cover practical information for users, including: General principles and rules; Key processes; Key performance and data quality metrics; Updates & next steps.

📊 Don't let simple mistakes ruin your clinical trial data! Check out our latest video for valuable tips on avoiding common errors in electronic data capture. Partner with diCELLa UNLIMITED for seamless EDC! 💪 #clinicaltrials

In our next webinar, “Discover more about how you can utilize IDBS Polar and Polar Insight to support your everyday analytical needs", learn how making data a core deliverable, rather than an afterthought, means getting the right people in the room, collecting the right information, and connecting seemingly disparate data points through a well-structured data backbone. Register now: https://ow.ly/Bntm50TwZ5Q #Biopharma #DigitalTransformation #DataManagement #IDBS Michael Barnes