Remove EHR Remove Groups Remove Meaningful Use Remove mHealth
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Three Big Questions for Stage 3 & Patient Engagement

Chilmark Research

For many, the delay of Stage 3 of the Meaningful Use program evoked a collective sigh of relief, providing a much-needed extra year to focus on the challenging requirements for patient engagement and interoperability. Each of these use cases brings with it a unique set of programmatic and technical components.

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FDA and Digital Health Regulation

Health Blawg

It is worth noting that the SaMD efforts are based on the principles articulated by a group of medical device regulators from around the world (IMDRF) which chartered a working group to look at SaMD; the IMDRF document was unanimously approved by its management committee and was adopted by the FDA. The Harlow Group LLC.

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FDA and Digital Health Regulation

Health Blawg

It is worth noting that the SaMD efforts are based on the principles articulated by a group of medical device regulators from around the world (IMDRF) which chartered a working group to look at SaMD; the IMDRF document was unanimously approved by its management committee and was adopted by the FDA. The Harlow Group LLC.

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FDA and Digital Health Regulation

Health Blawg

It is worth noting that the SaMD efforts are based on the principles articulated by a group of medical device regulators from around the world (IMDRF) which chartered a working group to look at SaMD; the IMDRF document was unanimously approved by its management committee and was adopted by the FDA. The Harlow Group LLC.

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FDA and Digital Health Regulation

Health Blawg

It is worth noting that the SaMD efforts are based on the principles articulated by a group of medical device regulators from around the world (IMDRF) which chartered a working group to look at SaMD; the IMDRF document was unanimously approved by its management committee and was adopted by the FDA. The Harlow Group LLC.

article thumbnail

FDA and Digital Health Regulation

Health Blawg

It is worth noting that the SaMD efforts are based on the principles articulated by a group of medical device regulators from around the world (IMDRF) which chartered a working group to look at SaMD; the IMDRF document was unanimously approved by its management committee and was adopted by the FDA. The Harlow Group LLC.

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Review of Mobile Devices and Health by Ida Sim in the NEJM

mHealth Insight

who is a Primary Care Physician, Professor at UCSF & coFounder at Open mHealth (follow her on Twitter @IdaSim ). mHealth Insights. Widely used in the social and behavioral sciences, EMA is an emerging method for outcomes assessment in both clinical care and clinical research. Authored by Ida Sim, M.D.,