Since the advent of artificial intelligence (AI), medical device manufacturers have been early adopters for product enhancements. Now, manufacturers are evaluating their regulated content and other production processes for suitable applications of AI and automation technology.
Moreover, while AI offers unprecedented opportunities for increased efficiency, accuracy and quality, it also requires a strong foundation of structured data and an awareness of global regulatory requirements. In this webinar, the expert speaker will discuss the importance of clinical and other data for effective AI development, as well as how some device makers are already employing machine learning and structured content to optimize process efficiency.
The highlights of this webinar include tangible benefits of AI-driven processes from real-world case study examples, key learnings from implementation and considerations for ensuring compliance. The speakers will also discuss the current challenges and opportunities, along with future trends, in the application of AI and other process automation technologies for regulated medical device content.
Join this webinar for an engaging discussion and to gain actionable insights into how to strategically implement AI and structured data to drive process automation.
Speakers
Sepanta Fazaeli, Clinical Systems & Medical Data Lead, Stryker
Sepanta Fazaeli serves as the Clinical Systems & Medical Data Lead at Stryker, where his expertise is applied in leveraging intelligent automation to enhance the quality, accessibility and utility of clinical and medical data.
At the heart of his role is leading a cross-functional collaboration within the Trauma & Extremities division, aiming to enhance operational efficiency and informed decision-making throughout the company. His efforts are crucial in integrating data solutions that are in sync with Stryker’s strategic goals, ensuring that progress in data management has a wide-reaching impact.
Message Presenter
Marc Miller, Division President, TransPerfect Medical Device Solutions
Marc Miller has over thirty years assisting all sizes of medical device manufacturers with translation and process automation for labeling, marketing, e-learning, software and other product-related content. He founded the first translation company certified to ISO 13485 and ISO 14971 and is a co-author of industry’s only risk management patent. In addition, he developed the first content automation system specifically designed to meet MDR and IVDR content requirements. Marc holds a BA from Harvard University and an MBA from Stirling University (Scotland).
Message Presenter
Laurent Meurens, Director, Europe, TransPerfect Medical Device Solutions
Laurent Meurens is the European Director of TransPerfect’s Medical Device Solutions division, bringing over a decade of experience in the language and technology industry. Since joining TransPerfect 7.5 years ago, he has been focusing on expanding the company’s medical device practice.
In his current role, Laurent works closely with medical device manufacturers to streamline and enhance their content creation and localization processes, leveraging advanced technology and AI to drive efficiency and innovation. Outside of work, Laurent enjoys running and exploring new destinations around the world.
Message PresenterWho Should Attend?
This webinar will appeal to professionals in the following fields:
- Medical device manufacturers
- Healthcare AI & automation
- Medical device
- Regulatory affairs
- Clinical operations
What You Will Learn
Attendees will learn about:
- What are the key technologies in a content automation workflow
- How leading MedTech companies are using AI-supported processes to automate clinical content creation and reduce translation and formatting costs
- How AI and structured data are changing the nature of global content creation
Xtalks Partner
TransPerfect Life Sciences
TransPerfect Life Sciences specializes in supporting global development and commercialization of drugs, treatments, and devices designed to improve and save lives. Our comprehensive solutions include eTMF and eClinical technologies, paper TMF migration, pharmacovigilance and safety solutions, translation and language services, and call center support. With offices in over 100 cities worldwide, TransPerfect is the ideal partner to ensure that your global launch makes a global impact. For more information, please visit our website at https://lifesciences.transperfect.com/.
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