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DiMe Testimonial

Katie Chowdhury Director at Global Regulatory Affairs | Medical Device Team | Digital Health, Emerging Tech and Combination Products at AbbVie

With the increasing role of software-based medical products, they are becoming ubiquitous and an important part of the fabric of technological advancements in healthcare. As a leader in bringing digital health products [particularly Software as a Medical Device (SaMD)] into a traditional drug-focused life sciences industry, it is more important an ever to collaborate and showcase SaMD development and its regulatory implications. Having various types of tools like the ones by DiMe’s RegPath will not only foster innovation in the field of SaMD, but will help thrive!”

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