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調査

ユーザー調査では、製品とユーザー間のインタラクション(相互作用)の質を左右する要因について、理解を深めることができます。 使用者のニーズや嗜好に関する見識は、ユーザーインターフェース要件に反映され、ユーザー中心設計に取り入れられます。 HFRDは、下記のような様々な方法で調査を行います。

​​観察調査で、お客さまの医療機器・体外診断用医療機器に対する使用者のニーズが判明します。

新しい機器や製品の使用者のニーズと嗜好を知るには、直接観察法が鍵となります。HFRDでは通常、観察中にあった意見やさまざまな作業時間を記録し、人と機器が干渉するポイントを文書に記録します。 例えば、麻酔科医がワークステーションで作業する様子を観察していた場合、「臨床医には注射の準備や書類の作成をするためのより大きな作業面が必要」等の報告内容をまとめます。

HFRDでは、世界中様々の調査ラボで働いた経験を持つ調査員と設計者が50人以上在籍しております。 コンコード(米国)、ユトレヒト(オランダ)、シカゴ(米国)にあるラボ、または、必要に応じてお客さまの施設で、調査を実施致します。

インタビューでは、総合的なユーザーフィードバックを提供致します。

HFRDの調査チームはさまざまなインタビュー技法を用いて、幅広いユーザーフィードバックを収集しております。下記はその例です。

  • デイリースタディ:デイリースタディなどのエスノグラフィー調査(行動観察調査)では、定性的なユーザー行動や製品使用の質的データを収集できます。

  • コンテキストインタビュー:ユーザーが作業をしている最中にインタビューをして、状況に合わせたフィードバックを収集します。

  • 1対1のインタビュー:面談や電話による個別インタビューで、個人のニーズや嗜好を深く掘り下げて調査します。
  • グループインタビュー: グループディスカッションは、観察調査や個別インタビューを補完する重要な調査です。グループインタビュー(フォーカスグループインタビュー)では、多くの意見を短時間で収集し、特定項目に対してグループ内での合意を得ることができます。

     

インタビュー結果は、観察やベンチマーク試験で得たデータを補完します。

ユーザビリティ試験を一歩進めるためのスタート地点が、ベンチマーク試験です。

既存機器のユーザビリティ試験を行うことで、使用者のニーズと嗜好について多くの情報を得ることができます。既存製品を、後継製品設計のための先行モデルとして試験することもあります。また、競合他社製品の性能試験を行い、ユーザーインターフェース要件やユーザビリティ目標のベースにすることもあります。
 

usability testing

医療機器ユーザビリティ調査で、規制関連リスクや患者のリスクを減らすことができます。

HFRDは、生命維持に使われる医療技術を重視したユーザー調査を数多く行っています。ユーザー調査を通じて、 規制当局の承認やビジネスゴールの達成をサポートすることが可能です。HFRDは、お客さまの機器に最適な調査手法を決定するお手伝いをし、お客さまの施設またはエマーゴのラボで調査を実施します。弊社は、新しいタイプの機器、高リスク医療機器、消費生活用製品、家庭用機器など、幅広い種類の製品を扱った経験があります。
 

ご質問がある方はこちらまで弊社スペシャリストへお問合せがある方はこちらまで

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ユーザー調査では、製品とユーザー間のインタラクション(相互作用)の質を左右する要因について、理解を深めることができます。

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弊社ヒューマンファクター「ツールキット」は、製品との心理的、物理的なインタラクション(相互作用)に重点を置いたさまざまな分析のパッケージです。

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医療機器UI(ユーザーインターフェース)設計にはユーザー調査を活用し、機能面でも美観においても目標の達成を目指します。

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総括的ユーザビリティ試験、形成的ユーザビリティ試験、専門家レビュー、ヒューリスティック分析、認知的ウォークスルー、等。

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エマーゴは、HFEのリサーチ、トレーニング、コンサルティング、プログラム開発を通して、より安全でより良い世界の実現に貢献します

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richard-featherstone

Richard Featherstone

調査ディレクター

Mary Burton

ユーザーエクスペリエンスディレクター
Allison Strochlic

Allison Strochlic

調査ディレクター

Merrick Kossack

調査ディレクター

Coming soon: Designing for Safe Use (CRC Press, late 2018)

by Kimmy Ansems, Cory Costantino, Alix Dorfman, Brenda Van Geel, Jonathan Kendler, Rachel Aronchick, Valerie Ng, Ruben Post, Jon Tilliss, and Michael Wiklund

We – this book’s authors/designers – are members of the Human Factors Research and Design (HFR&D) at EMERGO by UL. In this book, we have consolidated the lessons we have learned about designing for safe use, that is, designing products that shield people from harm to the extent possible.

We settled on a target of 100 principles on how to make products safer. The principles pertain to hardware, software, document, and document design. Yes, settling on an even one hundred principles was a bit arbitrary and cliché. The myriad ways to design for safe use do not stop sharply at one hundred. But, we think we covered many of the key ones.

We elected to use the term “product” broadly to cover things one might consider to be systems, machines, equipment, instruments, tools, applications, manuals, and instructions. These are all things that need to be designed properly to eliminate or reduce the chance of harm due to normal use and foreseeable misuse.

Most of the design principles could be addressed in an expanded form; even an entire book of its own. We choose brevity for the sake of communicating core concepts with some fun facts to spice things up.

As you read the book, be mindful that the science and art of making things safe is ever changing and that some of the content we present is sure to age. So, complement our guidance with insights you may gain from other sources, ranging from books to technical articles to standards and more.


Usability Testing of Medical Devices - Second Edition

by Michael Wiklund, Jonathan Kendler, and Allison Strochlic

Usability Testing of Medical Devices covers the nitty-gritty of usability test planning, conducting, and results reporting. The book also discusses the government regulations and industry standards that motivate many medical device manufacturers to conduct usability tests.

Since publication of the first edition, the FDA and other regulatory groups have modified their regulations and expectations regarding how medical device manufacturers should approach usability testing. Reflecting these changes, this Second Edition provides updated guidance to readers with an interest or direct role in conducting a usability test of a medical device or system. Key updates involve the 2011 FDA guidance on human factors engineering, requirements set forth by the third edition of IEC 60601 and closely related IEC 62366-1:2015, linking usability test tasks to risk analysis results, and analyzing root causes of use errors that occur during usability tests.

Written by seasoned human factors specialists, Usability Testing of Medical Devices, Second Edition is an informative, practical, and up-to-date handbook for conducting usability tests of medical devices. The book helps ensure a smooth and painless development process―and thus, safe and effective medical devices. Buy the book.


Writing Human Factors Plans and Reports for Medical Technology Development

By Michael Wiklund, Laura Birmingham, and Stephanie Larsen

This book provides the foundation for developing specific human factors engineering (HFE) work products that are needed to meet the FDA's human factors engineering (HFE) guidance. The authors have created a fictitious company and product to generate concrete examples of the plans and reports developed during various stages of HFE. The book includes an HFE project plan, a formative usability test plan and report, a summative (i.e., validation) usability test plan and report, and an HFE report. These work products and additional content outline the activities necessary to develop safe and effective medical devices, making this book an ideal resource for anyone interested in the medical technology field. Buy the book.


Medical Device Use Error Root Cause Analysis
by Michael Wiklund, Andrea Dwyer, and Erin Davis

This book offers practical guidance on how to methodically discover and explain the root cause of a use error―a mistake―that occurs when someone uses a medical device. Covering medical devices used in the home and those used in clinical environments, the book presents informative case studies about the use errors (mistakes) that people make when using a medical device, the potential consequences, and design-based preventions.

Using clear illustrations and simple narrative explanations, the text:

  • Covers the fundamentals and language of root cause analysis and regulators’ expectations regarding the thorough analysis of use errors
  • Describes how to identify use errors, interview users about use errors, and fix user interface design flaws that could induce use errors
  • Reinforces the application of best practices in human factors engineering, including conducting both formative and summative usability tests 

Buy the book


Handbook of Human Factors in Medical Device Design

Edited by Matthew Weinger, Michael Wiklund, and Daryle Gardner-Bonneau

Developed to promote the design of safe, effective, and usable medical devices, Handbook of Human Factors in Medical Device Design provides a single convenient source of authoritative information to support evidence-based design and evaluation of medical device user interfaces using rigorous human factors engineering principles. It offers guidance on user-centric design supported by discussions of design issues, case studies, and examples. The book sets the foundation with coverage of fundamental topics such as aligning the interactive nature of medical devices to the expected use environments ranging from hospitals and ambulances to patients’ homes, drawing on anthropometric and biomechanical data to ensure that designs match the intended users’ bodies and physical abilities, and conducting usability tests and other evaluations to ensure that devices perform as intended. It then focuses on applied design issues, offering guidance on the design of specific types of devices and designing devices for particular use environments. Adapted in part from established design standards and conventions, the design guidance presented in this work distills professional judgment extracted from the contributing authors’ years of experience in applied analysis and design. Written in true handbook style, each chapter stands alone and includes tables, illustrations, and cross references, allowing you to quickly find the exact information you need. Most chapters begin with a general introduction to the selected topic, followed by the presentation of general and special design considerations and then specific, numbered design guidelines. The book also presents a listing of resources, literature, and website references. It not only focuses on the human factors issues that arise when developing medical devices, it supplies the necessary guidance to resolve them. Buy the book.


Designing Usability into Medical Products
by Michael Wiklund and Stephen Wilcox

Advocating a user-centered approach to medical technology design, Designing Usability into Medical Products covers the essential processes and specific techniques necessary to produce safe, effective, usable, and appealing medical systems and products. Written by experts on user-centered research, design, and evaluation, the book provides a range of alternative approaches to the subject. Wiklund and Wilcox explore how to make medical devices safe and effective by involving users in the design process. They discuss specific design and evaluation methods and tools, present case studies of user-friendly medical technologies and corporate human factors programs, and supply related resources for medical design professionals.

The book conveys an in-depth understanding of the user-centered design process, covers design methods for FDA compliance, and offers guidance on performing a variety of hands-on user research, user interface design, and user interface evaluation. The authors make a compelling case for treating the user's needs and preferences as a top design priority, rather than an afterthought. They demonstrate that high-quality customer interactions with systems and products leads to effective medical diagnosis and treatment, increases the physical and mental well being of patients and caregivers, and leads to commercial success in a crowded marketplace. Buy the book.


Usability in Practice

Editor: Michael Wiklund

This volume investigates how major corporations, such as Microsoft, Borland, Apple, Eastman Kodak, and Silicon Graphics, address usability issues. It presents case studies of each organization, outlining their program structures, program goals, and team members' responsibilities and resources. The book also addresses how usability is marketed inside the organization and to customers, as well as the lessons learned during the course of product development efforts. Each illustrated study includes advice that should help readers establish and manage their own program.

Out of print. Used copies might be available.


The Beauty of Unity-in-Variety

by Ruben Post

Products have the capacity to evoke a sense of beauty or appreciation in us. Whether marveling over a new car, admiring the interface of our next generation smartphone, or wielding a perfectly balanced kitchen knife, we can appreciate perceiving their design. The features of an artifact, arranged and produced from following a plan. However, most of us are rarely aware of what exactly makes a certain product aesthetically appealing – or that aesthetically pleasing products are generally considered more usable as well. This thesis studies how our aesthetic appreciation of products is formed in the visual and tactile sensory domain. It identifies how unity (the degree to which a design comes across as ordered, coherent, and structured as one whole) and variety (the degree of differences, diversity, and number of elements in a design) can together explain our aesthetic appreciation for products. Furthermore, it identifies ways to influence unity and variety to create the most aesthetically pleasing designs.

Available at Institutional Repository, Delft University in Delft, The Netherlands. Contact Ruben Post at ruben.post@ul.com.