Jul 17, 2019

Études des facteurs humains : Considérations relatives au recrutement de populations d'utilisateurs rares et complexes

Conseils à l'intention des enquêteurs de l'étude de validation des facteurs humains qui recrutent des utilisateurs représentatifs.
Jul 10, 2019

Human factors studies: Considerations for recruiting rare and complex user populations

Tips for human factors validation study investigators recruiting representative user participants
Jun 5, 2019

Human factors engineering: Expense or investment?

Embedding human factors engineering (HFE) and usability studies early in medical device design and development cycles can yield benefits beyond regulatory compliance for manufacturers.
May 21, 2019

La conception de dispositifs médicaux connectés pour l'Internet des objets

Par Joe Fegelman et Natalie Shortt LES POINTS PRINCIPAUX PAR EMERGO by UL La conception...
May 8, 2019

Connected medical device design for the Internet of Things

EMERGO BY UL SUMMARY OF KEY POINTS: Connected medical device design and develoment paradigm shifting...
Apr 1, 2019

GDPR and human factors studies for medical devices: Key issues for manufacturers and sponsors

EMERGO BY UL SUMMARY OF KEY POINTS: The European GDPR has ramifications for how medical device human factors researchers collect and manage data related to study participants, even outside of the EU. Human factors researchers should work with their clients (if they serve in a consulting capacity) and other third parties (e.g., vendors) to define roles and responsibilities early during study planning and develop best practices that comply with GDPR requirements. All participant data management decisions and rationales should be properly documented to demonstrate GDPR compliance.
Mar 14, 2019

Fatal Medical Error: Too common to investigate thoroughly?

EMERGO BY UL SUMMARY OF KEY POINTS: Investigations of preventable medical errors in the US healthcare system in need of revamp; Scale of fatal medical errors hindering more rigorous investigations; Multidisciplinary approach incorporating human factors components needed to address ongoing medical use errors.
Feb 27, 2019

Dealing with usability test no-shows, cancellations, and late participants

EMERGO BY UL SUMMARY OF KEY POINTS: Medical device usability test administrators are often challenged by no-show participants. Steps such as overrecruiting, rescheduling and partial participation allowances can help mitigate this challenge.
Feb 23, 2019

Quand une spécialiste des facteurs humains devient le patient

Par Allison Strochlic LES POINTS PRINCIPAUX PAR EMERGO by UL : Les dispositifs médicaux conçus et mis au point pour les utilisateurs finaux cliniques négligent souvent le facteur de l'expérience du patient. Les professionnels de l'IFH et de l'aptitude à l'utilisation devraient tenir compte de l'impact de leurs conceptions non seulement pour les cliniciens, mais aussi pour les patients destinataires de tels dispositifs. La conception d'instruments et de systèmes qui favorisent une meilleure expérience positive pour les patients mérite une attention particulière.
Feb 14, 2019

인간 공학 전문가가 환자가 되면 생기는 일

EMERGO BY UL 핵심 요약: 의료기기는 최종 사용자인 의사를 위해 설계 및 제작되며, 환자 경험 요인은 간과되기 쉽습니다. 인간 공학(HFE) 및 사용 편의성 전문가들은 자신의 설계가 의사뿐 아니라 해당 의료기기를 통해 치료 및 모니터링을 받는 환자에게 미치는 영향에 대해서도 고려해야 합니다. 긍정적인 환자 경험을 불러오는 의료기기 및 시스템 설계에 더욱 주목해야 합니다.

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