On-Demand
Trusted Automation Meets IVDReadiness
- Time
- 1 hour
Clinical laboratories rely on precision, consistency, and speed to deliver reliable results that directly impact patient care. But as workflows grow more complex, maintaining control, traceability, and efficiency becomes increasingly challenging.
That’s where automation changes the game.
Laboratory automation platforms help labs standardize and automate critical workflow steps - reducing manual handling, minimizing variability, and building highly reproducible processes across even the most demanding diagnostic applications. The result: stronger operational performance, greater efficiency, and dependable process control.
At the same time, the European In Vitro Diagnostic Medical Devices Regulation (IVDR, Regulation (EU) 2017/746) raises the bar for laboratories especially developing and using in-house IVDs. It’s not only about running controlled workflows - labs must also prove and document compliance evidence in a structured, transparent, and audit-ready way. This creates an opportunity to strengthen process standardization, improve traceability, and establish objective documentation of compliance.
Learn how automation and documentation come together to close the gap between the lab and compliance. Discover how to streamline and standardize laboratory workflows, while transforming regulatory data into structured, IVDR-ready technical documentation. Get insights on how combining Hamilton’s automated lab workflows with Platomics’ digital documentation platform PlatoX® can cut manual effort, strengthen traceability, and create a scalable, end-to-end path operational excellence and to IVDR compliance.
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Speakers
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Andreas Oberleitner, MSc.
VP of Regulatory Affairs, Platomics GmbH -
Dr. Frank Streckenbach
Market Segment Manager Genomics & Multiomics, Hamilton