Kitty Makra, Director, Digital Strategy
Yena Lee, Director of AI Strategy
2022-12-01

How to launch your SaMD to market faster

At our third Software as a Medical Device meetup, Danielle Dorfman Faruq (Regulatory & Quality Director at Kintsugi) shared learnings and tips on how to get your SaMD in the hands of real users faster, while meeting regulatory requirements.

animated doctor
Yena Lee, Director of AI Strategy
Gustavo Oregel, Principal - Visual & Motion Design
2022-09-26

Motion graphics are an effective way to add visual interest to any website or app. They're also a great way to highlight key points in your content and improve patient compliance. We've put together examples of how motion graphics can be used effectively in digital therapeutics.

Venn diagram overlapping a mobile device
Kitty Makra, Director, Digital Strategy
Yena Lee, Director of AI Strategy
2022-09-20

Last week at our second SaMD meetup, we discussed how to apply agile product management strategies to building and validating digital therapeutics.

a web connecting people with healthcare and technology
Yena Lee, Director of AI Strategy
Kitty Makra, Director, Digital Strategy
2022-09-09

At Rangle, we’re creating a community for innovators in the software as a medical device (SaMD) space.

roadmap through a stethoscope around a mobile phone
Yena Lee, Director of AI Strategy
2022-08-22

A core component of a premarket submission is clinical evidence. Clinical evidence is gathered through a process of clinical validation, which involves gathering data on the safety and effectiveness of the product. The overarching goal of clinical validation is to demonstrate to regulators that the device will work, as intended, for target users.

roadmap through a stethoscope around a mobile phone
Yena Lee, Director of AI Strategy
2022-08-22

A core component of a premarket submission is clinical evidence. Clinical evidence is gathered through a process of clinical validation, which involves gathering data on the safety and effectiveness of the product. The overarching goal of clinical validation is to demonstrate to regulators that the device will work, as intended, for target users.

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