Discover Effective AI Strategies for Medical Devices in Free Webinar

A free webinar titled “Process AI in Medical Devices: What Works and What’s Next” is set to take place on December 11, 2025, at 11:00 AM EST, hosted by Xtalks. This event aims to educate medical device manufacturers on how to utilize artificial intelligence (AI) in clinical and regulatory processes, known as Process AI, to achieve scalable and compliant automation.

Participants will gain valuable insights into the essential components, risks, and advantages of establishing an “AI Center of Excellence” for translating clinical and regulatory content. The featured speakers, including Marc Miller, Division President of TransPerfect Medical Device, and Sepanta Fazaeli, Head of AI Solutions for Life Sciences at TransPerfect Life Sciences, will share their expertise on overcoming common pitfalls that lead to AI initiatives failing to scale.

Research from QServe Group and TransPerfect Medical Device indicates that while 70% of manufacturers express dissatisfaction with current AI outcomes, many are uncertain about effectively implementing AI in regulated environments. This session aims to tackle that uncertainty by showcasing where Process AI has already demonstrated measurable benefits, particularly in AI-supported translation and linguistic quality assurance workflows. These applications enhance consistency, accuracy, and compliance in the face of increasing regulatory demands under the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR).

Despite its potential, Process AI faces challenges, particularly concerning large language models (LLMs). Issues such as reproducibility, factual reliability, and explainability persist, and existing techniques have not yet resolved these fundamental problems. The future of AI in medical devices lies not in pursuing the latest models but in developing frameworks that enable the appropriate model to be applied to each specific use case.

In the upcoming session, the speakers will first explore the current success of Process AI through language workflows, translation, and linguistic QA. These areas have shown substantial improvements, reducing translation costs and time by 30-40% while ensuring compliance and traceability. While LLMs can assist with terminology and quality control, their variability necessitates validated guardrails to ensure reliability.

The webinar will also address the application of Process AI across various life sciences operations. Instead of treating processes such as post-market surveillance, complaint handling, and regulatory content authoring as isolated AI projects, attendees will learn how to integrate core tasks like classification, extraction, summarization, and generation. This approach allows for the creation of reviewer-ready and compliant systems that can scale effectively.

To register for the webinar and learn how Process AI can streamline operations for medical device manufacturers, visit the event page. The session promises to equip professionals with the knowledge needed to integrate AI into their daily clinical and regulatory workflows successfully.

Xtalks, powered by Honeycomb Worldwide Inc., is a prominent provider of educational webinars and digital content for the global life sciences community. Each year, thousands of industry professionals turn to Xtalks for insights into regulatory developments and best practices. For further information about Xtalks or hosting a webinar, please contact Vera Kovacevic at +1 (416) 977-6555 x371 or via email at [email protected].