AAMI HE74 : 2001 : R2009
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
HUMAN FACTORS DESIGN PROCESS FOR MEDICAL DEVICES
Hardcopy , PDF
09-01-2021
English
01-01-2009
Committee representation
Foreword
Introduction
1 Scope
1.1 The benefits of HFE
1.2 Avoiding design-induced error
1.3 Improving usability
2 Normative references
3 Definitions
4 Overview of the HFE process
4.1 Iterative nature of the HFE cycle
4.2 User research
4.3 Design concept development (conceptual design)
4.4 Design criteria and requirements development
4.5 Detailed design and specification
4.6 Design evaluation
4.7 Design implementation and deployment
5 Planning the HFE process
5.1 Assuring adequate HFE involvement in the design team
5.2 Scaling the HFE effort
5.3 Documenting the HFE activities
6 The HFE process: A systems approach
6.1 User input
6.1.1 Sampling users
6.1.2 Research protocols and informed consent
6.2 Design criteria and requirement development
6.3 Device design
6.3.1 Structuring an approach to design
6.3.2 Modeling the user interface
6.4 Design specifications
6.4.1 Hardware user interface specifications
6.4.2 Software user interface specifications
6.4.3 Other useful HFE tools
6.5 Design evaluation
6.5.1 Design verification
6.5.2 Production unit validation
7 Methods and techniques used in the HFE process
7.1 Cognitive walkthrough
7.2 Contextual inquiry and observation
7.3 Design audits
7.4 Device comparisons and functional analysis
7.5 Expert reviews
7.6 Functional analysis
7.7 Heuristic analysis
7.8 Interviews
7.9 Participatory design
7.10 Prototyping
7.11 Questionnaires and surveys
7.12 Simulated clinical environments and field testing
7.13 Task analysis
7.13.1 Time-and-motion studies
7.13.2 Cognitive task analysis
7.14 Usability testing
7.15 Use error analysis
7.16 Workload assessment
8 The complementary role of other types of analysis
8.1 Risk analysis
8.2 Cost-benefit analysis
Annexes
A Rationale for the development and provisions of this standard
B Current FDA regulations
C Helpful tips
D References
E Bibliography
Provides an overview of the human factors engineering (HFE) discipline, a discussion of the benefits of HFE, a review of the HFE process and associated analysis and design techniques, and a discussion of implementation issues and relevant national and international standards and regulations.
Committee |
HE
|
DevelopmentNote |
Supersedes AAMI HE48. (02/2010)
|
DocumentType |
Standard
|
Pages |
48
|
ProductNote |
Reconfirmed 2009
|
PublisherName |
Association for the Advancement of Medical Instrumentation
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
ISO 9241-11:1998 | Ergonomic requirements for office work with visual display terminals (VDTs) Part 11: Guidance on usability |
AAMI HE48 : 1993 | HUMAN FACTORS ENGINEERING GUIDELINES AND PREFERRED PRACTICES FOR THE DESIGN OF MEDICAL DEVICES |
ISO 9241-17:1998 | Ergonomic requirements for office work with visual display terminals (VDTs) Part 17: Form filling dialogues |
ISO 9241-10:1996 | Ergonomic requirements for office work with visual display terminals (VDTs) Part 10: Dialogue principles |
MIL-HDBK-46855 Revision A:1999 | HUMAN ENGINEERING PROGRAM - PROCESS AND PROCEDURES |
CLSI GP19 P : 1994 | LABORATORY INSTRUMENTS AND DATA MANAGEMENT SYSTEMS: DESIGN OF SOFTWARE USER INTERFACES AND SOFTWARE SYSTEMS VALIDATION, OPERATION, AND MONITORING |
CFR 45(PTS1-199) : OCT 2017 | PUBLIC WELFARE - SUBTITLE A - DEPARTMENT OF HEALTH AND HUMAN SERVICES - GENERAL ADMINISTRATION - SUBTITLE B - REGULATIONS RELATING TO PUBLIC WELFARE |
ISO 9241-12:1998 | Ergonomic requirements for office work with visual display terminals (VDTs) Part 12: Presentation of information |
MIL-HDBK-759 Revision C:1995 | HANDBOOK FOR HUMAN ENGINEERING DESIGN GUIDELINES |
MIL-HDBK-1908 Revision B:1999 | Definitions of Human Factors Terms |
ISO 9241-16:1999 | Ergonomic requirements for office work with visual display terminals (VDTs) Part 16: Direct manipulation dialogues |
ISO 9002:1994 | Quality systems — Model for quality assurance in production, installation and servicing |
ISO 9241-14:1997 | Ergonomic requirements for office work with visual display terminals (VDTs) — Part 14: Menu dialogues |
ISO 9241-15:1997 | Ergonomic requirements for office work with visual display terminals (VDTs) Part 15: Command dialogues |
ANSI HFS100 : 1988 | HUMAN FACTORS ENGINEERING OF VISUAL DISPLAY TERMINAL WORKSTATIONS - AMERICAN NATIONAL STANDARD FOR |
CFR 21(PTS1-99) : 0 | FOOD AND DRUGS - FOOD AND DRUG ADMINISTRATION, CHAPTER 1 DEPARTMENT OF HEALTH AND HUMAN SERVICES - PARTS 1-99 |
ISO 9001:2015 | Quality management systems — Requirements |
MIL-STD-1472 Revision G:2012 | HUMAN ENGINEERING |
AAMI ISO 13488 : 1996 | QUALITY SYSTEMS - MEDICAL DEVICES - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF ISO 9002 |
AAMI/ISO 13485:2016 | MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - REQUIREMENTS FOR REGULATORY PURPOSES |
ISO 9241-13:1998 | Ergonomic requirements for office work with visual display terminals (VDTs) — Part 13: User guidance |
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