The persistence of PFAS in the environment and potential health risks have led to regulatory actions affecting the medical device industry. In this blog, learn key PFAS details and how to address PFAS challenges for medical device companies.
Streamlining the Path to Market for Generic Drug-Device Combinations
Generic drugs play an important role in healthcare, but bringing them to market can be complex, cost-prohibitive, and time-consuming. This six-phase approach to creating generic drug-device combination products (g-DDCPs) aims to simplify the process.
AI: The New Partner in Medical Device Development
Learn how AI technologies evolved throughout the years, how Battelle used (and is using) AI to develop life-changing medical devices, and how to responsibly advance medical device innovation in the "AI Age".
The Growing Concern of Transformation Products (TPs)
During the water treatment process, contaminants such as transformation products (TPs) can emerge. Learn more about transformation products, why they matter and what Battelle can do to help.
The Role of Psychology in Medical Device Training Design
Discover how psychology can inform user training for medical devices, and learn the top 6 psychological principles for effective training design.
The Impact of PFAS Regulations on the Medical Device Industry
Discover the effect of PFAS regulations on the medical device industry, and explore our experts' 5 strategies to help medical device companies adapt to this evolving landscape.
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