Remote Work as a Societal Incentive for Creativity: Phygital Initiative for Self-actualization

Burova, Natalia V.; Molodkova, Eleonora B.; Николаенко, А. В.; Popazova, Olga

doi:10.1007/978-3-030-89708-6_15

Cited by 2 publications

(1 citation statement)

References 27 publications

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“…As a neologism (merging two words: physical and digital), this attribute has been typically adopted across various domains like design and marketing, blending real and virtual dimensions as in its etymology (Gaggioli, 2017 ; Mikheev et al, 2021 ). This term was used, for instance, to define Tactile User Interfaces (TUIs) like the “phygital map” in Nakazawa and Tokuda ( 2007 ), the paradigms of “phygital play” (Lupetti et al, 2015 ) in mixed reality-based robotic games (MRRGs) (Prattico and Lamberti, 2020 ), and interactive solutions for work and education proposed during the COVID-19 pandemic (Chaturvedi et al, 2021 ; Burova et al, 2022 ).…”

Section: Phygital Twins In Human-robot Interactionmentioning

confidence: 99%

Beyond Digital Twins: Phygital Twins for Neuroergonomics in Human-Robot Interaction

et al. 2022

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Section: Phygital Twins In Human-robot Interactionmentioning

confidence: 99%

Beyond Digital Twins: Phygital Twins for Neuroergonomics in Human-Robot Interaction

et al. 2022

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Is medical device regulatory compliance growing as fast as extended reality to avoid misunderstandings in the future?

Bini,

Franzò,

Maccaro

et al. 2023

Health Technol.

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Purpose European Extended Reality (XR) industry is expected to significantly increase by 2025 with an extreme impact on the Healthcare scenario. Considering that the transition period for the Medical Device Regulation 2017/745 (MDR 2017/745) will end in May 2024, purpose of this study is to assess whether the Medical Device Regulatory Compliance is ready to cope with the inclusion of XR and its possible social and economic impact in the world of medical device software (MDSW). Methods XR publications patterns were evaluated since MDR 2017/745 release on different databases. European normative about MDSW are consulted, followed by the European Database of Medical Devices (EUDAMED). Results The number of publications on XR have increased since 2017 and healthcare is the third highest-impacted subject area. Specific classes for software have been introduces in the European Nomenclature of Medical Devices (EMDN) and some XR applications have already been registered in EUDAMED classified as MDSW. Conclusions XR will become intrinsic in everyday medical protocol and guidelines. The establishment of the IEEE Virtual Reality and Augmented Reality Working Group and the statement of VR for remoting surgery as a MDSW in MDCG 2019-11 are demonstration of the necessity of MD regulatory compliance in being able to keep up with the upcoming XR technologies. The Authors agree that the competent authorities should consider intervening in the European Regulative Compliance to cope with the revolution of Phygital in Healthcare and to regulate procedures involving the use of XR in medicine preventing future misunderstanding and criticalities especially for high risk situations.

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Remote Work as a Societal Incentive for Creativity: Phygital Initiative for Self-actualization

Cited by 2 publications

References 27 publications

Beyond Digital Twins: Phygital Twins for Neuroergonomics in Human-Robot Interaction

Beyond Digital Twins: Phygital Twins for Neuroergonomics in Human-Robot Interaction

Is medical device regulatory compliance growing as fast as extended reality to avoid misunderstandings in the future?

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