Digital Medicine Society (DiMe)

A Digital Medicine Society (DiMe) is a non-profit organization that is a professional society dedicated to the development of digital medicine.

• Context:
  • Website: https://www.dimesociety.org
• Example(s):
  • DiMe's Crowdsourced Library of Digital Endpoints,
  • DiMe Webinar Series,
  • DiMe Virtual Journal Club,
  • …
• Counter-Example(s):
  • Association of Clinical Research Organizations (ACRO),
  • Association of Clinical Research Professionals (ACRP),
  • Clinical Trials Transformation Initiative (CTTI),
  • Decentralized Trials & Research Alliance (DTRA),
  • Medable Incorporated,
  • TransCelerate Biopharma Incorporated.
• See: Decentralized Autonomous Organization (DAO), Decentralized Clinical Trial, COVID-19, Telemedicine, Decentralized Networking System, Decentralized Application (DApp).

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References

2021a

• (DiMe, 2021) ⇒ https://www.dimesociety.org/about-us/ Retrieved: 2021-10-2.
  • QUOTE: Founded in 2019, the Digital Medicine Society (DiMe) is the first professional organization for experts from all disciplines comprising the diverse field of digital medicine.

    DiMe is a 501c3 nonprofit that exists to advance the safe, effective, equitable, and ethical use of digital medicine to optimize human health.

2021b

• (De Beuckelaer, 2021) ⇒ Erwin De Beuckelaer, J.J. Ferrer, Kris Karson, Lorcan Walsh, Philip-Moritz Russmeyer, Rachel Chasse, Shwen Gwee, Tim Ruckh, Elisa Frenz, and Chandana Fitzgerald. "Digital Health Vendor Assessment For Clinical Trials". In: DiMe Publications.
  • QUOTE: HealthXL and a consortium of representative stakeholders from across the digital health ecosystem have been working to advance the understanding and adoption of digital health products used in clinical trials. To reduce variable implementations of similar quality standards, the interdisciplinary group began in Q4 2020 to work towards an open-source industry guidance to facilitate vendor qualification for clinical trials. With a standardized template, vendors will have a response package prepared with most of the expected documentation in a format that sponsors are ready to accept and review. This framework is meant to serve as a guidance for industry but can easily be adapted to suit individual needs and specifications.

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