MDIC Studio Panel: Challenges to Adopting Advanced Manufacturing in MedTech

Join industry leaders Domhnall Caroll, CEO of Digital Manufacturing Ireland, Garth Conrad, Vice President of Quality at Flex Health Solutions, Daniel Matlis, CEO and Founder of Axendia, and Francisco Vicenty, Case for Quality Program Manager at the FDA CDRH in a compelling discussion on the adoption of advanced manufacturing in the medical device field. Discover how companies are tackling barriers such as ROI and internal expertise, common fears and misconceptions industry has on advanced manufacturing, and how regulatory agencies are evolving their approach. Watch the panel and discover how participating in the Advanced Manufacturing Clearing House can improve overall quality and product safety.

The purpose of Advanced Manufacturing Clearing House is to encourage Medical Device Industry to adopt advanced technology across the total product life cycle. Objectives include improving design, supply, production, distribution, tracking, device reliability, overall quality, and safety across the product life cycle. Examples of advanced technologies include but not limited to additive and generative part design, digital twins, and digital threads (e.g., modeling and simulation for virtual design verification, validation and design transfer), and data-driven closed-loop quality.

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Cover Image Provided Courtesy of FLEX Health Solutions