Process AI in Medical Device: What Works and What’s Next

Research from QServe Group and TransPerfect Medical Device asked manufacturers how they are utilizing AI in their clinical and regulatory processes (Process AI).

Although 70% report not being fully satisfied with current outcomes, many manufacturers are unsure how to apply AI effectively in regulated environments.

This session will address that challenge by highlighting where Process AI is already delivering measurable value, such as in AI-supported translation and linguistic quality assurance workflows that improve consistency, accuracy and compliance.

Driven by the increased regulatory demands under MDR and IVDR, Process AI is being utilized or evaluated by over 48% of manufacturers surveyed across regulatory, clinical and training/education.

Yet challenges remain: large language models (LLMs) struggle with reproducibility, factual reliability and explainability.

Specialized techniques like scaling parameters, stacking reasoning layers or chaining agents haven’t solved these basic issues. The path forward lies not in chasing the newest model but in creating a development framework that allows the right model to be applied to each use case.

In this session, the featured speakers will first discuss where and how Process AI is working today through language workflows, translation and linguistic QA. These areas are where neural-engine training, human-in-the-loop review and real-time quality monitoring deliver measurable results, reducing translation cost time by 30-40% while maintaining traceability and compliance. LLMs can assist with terminology and QC, but their variability requires validated guardrails.

The webinar will also explore the use of Process AI across life sciences operations. Instead of treating each process, such as post-market surveillance, complaint handling, systematic literature review and regulatory content authoring, like separate AI projects, this session will show how the same core tasks (like classification, extraction, summarization and generation) can be mixed and matched. With these building blocks in place, attendees will be able to create reviewer-ready, compliant systems that can scale.

Register for this webinar to learn how Process AI enables scalable, compliant automation for medical device manufacturers.

You can register for the live event and get access to the recording here: https://xtalks.com/webinars/process-ai-in-medical-devices-what-works-and-whats-next/