This outline proposes using human factors engineering (HFE) to reduce medication administration errors by nurses. The introduction explains that the project will analyze errors at the author's workplace to identify root causes, such as interruptions and a lack of standard processes. Potential HFE countermeasures include standardizing work, using visual cues, and electronic verification. The conclusion will assess how well the countermeasures reduced errors.
This presentation will give insights in importance of ergonomics, and time and motion study in designing workplace and how an ergonomically designed workstation/workplace impacts on productivity of operators/workers.
This presentation gives suggestions with examples on how to evaluate workplace for lighter assembly works and how cycle time can be reduced for specific jobs
Modern Computing: Cloud, Distributed, & High Performanceinside-BigData.com
In this video, Dr. Umit Catalyurek from Georgia Institute of Technology presents: Modern Computing: Cloud, Distributed, & High Performance.
Ümit V. Çatalyürek is a Professor in the School of Computational Science and Engineering in the College of Computing at the Georgia Institute of Technology. He received his Ph.D. in 2000 from Bilkent University. He is a recipient of an NSF CAREER award and is the primary investigator of several awards from the Department of Energy, the National Institute of Health, and the National Science Foundation. He currently serves as an Associate Editor for Parallel Computing, and as an editorial board member for IEEE Transactions on Parallel and Distributed Computing, and the Journal of Parallel and Distributed Computing.
Learn more: http://www.bigdatau.org/data-science-seminars
Watch the video presentation: http://wp.me/p3RLHQ-ghU
Sign up for our insideHPC Newsletter: http://insidehpc.com/newsletter
Management of Library Automation
Library Automation refers to the use of computers to serve the needs of library users. The operations of a library get a quantum jump with the introductions of computers. The computers help to provide fast and reliable access to the resources available in the library as well as elsewhere. The application of computers in the library operations avoids repetitive jobs and saves lot of labour, time, speeds up operations, increases use of library resources. Computers are not only used as a tool for processing the data, but also for data storage and accessing. Planning for an automated system, no matter how big or small, should be part of an overall long-range plan for the library. Automation should always be used as a means to achieve overall better patron service.
Library Automation refers to the use of computers to serve the needs of library users. The operations of a library get a quantum jump with the introductions of computers. The computers help to provide fast and reliable access to the resources available in the library as well as elsewhere. The application of computers in the library operations avoids repetitive jobs and saves lot of labour, time, speeds up operations, increases use of library resources. Computers are not only used as a tool for processing the data, but also for data storage and accessing. Planning for an automated system, no matter how big or small, should be part of an overall long-range plan for the library. Automation should always be used as a means to achieve overall better patron service.
Curation-Friendly Tools for the Scientific Researcherbwestra
Presentation for Online Northwest Conference, in Corvallis Oregon, February 10, 2012.
Highlights electronic lab notebooks (ELN) and OMERO (Open Microscopy Environment) as two tools that enable researchers to better manage their research data.
Requirements engineering scenario based software requirement specificationWolfgang Kuchinke
Requirements Engineering – Writing the Software Requirements Specification (SRS). A CRI Group Workshop. The requirements engineering approach employed successfully in the EHR4CR process is shown and discussed in order to extract lessons learned and to use it for new projects.
Requirements engineering is the process of eliciting stakeholder needs and desires and develope them into an agreed set of detailed requirements. It serves as basis for all subsequent software development activities.
In general, a project begins with the requirement acquisition phase and ends with the specification of requirements in form of the Software Requirement Specification (SRS). Requirements specification may even be used to manage the consistency of the entire system.
Learning from the Requirements Engineering process in the the EU project EHR4CR. Especially the topics of Requirements Scenarios in the process of requirement gathering and the iterative writing and validation of software requirements specification (SRS) document can be applied to new projects. The Requirements Process consists of 4 steps: Requirements Elicitation – the art to receive meaningful requirements. Requirements Analysis – iterative improvement of quality of requirements. Writing the Requirements Specification document (Software Requirement Specification) and Requirements Validation - this is also done iteratively with several workshops.
Novel is the introduction of an iterative process for requirements engineering. Start with only a subset of software requirements, iterate the collection and validation until the full system is implemented. In each iteration, design modifications are made and new functional capabilities are added. Following tools for requirements gathering were used: Use Cases, Descriptions of current situation and workflow, Context diagram, Stakeholder interviews, Scenarios and Use Case workshops.
A novel scenario based approach for requirements engineering is being introduced: The domain scenario is used to estimate probable effects (situation analysis and long-range planning). The domain scenario is broken down into high-level "Usage Scenarios". Usage Scenarios describe critical business interactions and their anticipated operations; they serve as context for the use cases and the generation of requirements; they make sure requirements are complete.
Development of the SRS with involvement of scenarios: 1. Begin with Domain Scenarios; 2. Development of Usage Scenarios; 3. Software Requirements Specification document. Several round of change management were employed during writing the SRS. This possibility for correction and improvement ensured that the requirements are of high quality and applicability.
Diagnostic hypothesis refinement in reproducible workflows for advanced medic...Cezary Mazurek
(1) In-Silico experiments, especially in their refinement cycle, lead to creation of new software tools, algorithms and even computer science challenges. To make this experiment valuable such a process need to be controlled and recorded while achieving milestone stages;
(2) Scientific experiments are performed in cycles, when each cycle is a refinement of hypotheses. Continuing research starting from any cycle and branching this process further on, require that each cycle is checkpointed and stored as a scientific procedure step;
(3) Medical research reliant on data analysis, focused on early disease diagnosis or stopping the disease progress, very often results in providing software tools helping in data analysis and created during the experimentation cycles. To treat the process of knowledge discovery based on data analysis and development of processing tools, as a research method, we need to provide the way of formal description of stages of such a process, be paired with hypothesis refinement stages.
‐ Total Assessment Weighting ‐ 25 Introduction T.docxodiliagilby
‐ Total Assessment Weighting ‐ 25%
Introduction:
The optimisation of processing times is an important skill for all engineers and is often undertaken
via a modelling approach. The processing of composites can be a long process and a bottleneck in a
production line. The temperature profile during the composite cure can be adjusted to reduce
processing time and increase part output during production.
The quality control of composites is also time consuming and costly. Most non-destructive testing is
inconclusive, so thermal and mechanical testing is conducted to ensure quality is consistent.
Choosing the most cost and time effective method is critical to meet high standards in an efficient
way.
This assessment task is based on experimental work performed during Practical 1. You will be
creating a ‘technical research paper’ based on your composite experiments performed during week
2 and 3.
Assessment task:
In Practical 1 you performed a set of experiments related to optimizing the manufacture of
composites. Using the template provided, you will create a technical research paper based around
these three experiments. Please read the template carefully in terms of how to write and structure
your technical paper. Your paper will discuss the following elements.
1) Calculation of Kinetic and Rheology Constants: Using information in the literature and unit
content, use data generated from a Differential Scanning Calorimetry (DSC) and/or
Rheometer to find the constants to be used for the modelling of viscosity curves. A proposal
of potential alternative solutions to create a model for resin viscosity is to also be presented.
2) Optimisation of flow through a fibre stack: based on your observations from the practical
and from the experimental data collected, you will use the rheology model created to
optimise the temperature profile for increased flow of resin through a fibre stack, and
predict the time it will take to reach the tool surface and wet out the fibre tack surface.
3) Quality Control Testing: Recommend and justify a test procedure to measure the following
key properties of a manufactured component:
• Glass Transition Temperature
• Tensile modulus
• Internal porosity
• Bond between carbon fibre plies
• Degree of cure/conversion percentage
• Fatigue
• Fatigue at temperature
Discuss whether the recommended procedure is standardised, the data that needs to be
collected and calculations that need to be made.
Writing the Report:
You are welcome to use the recommended title template below as a guide to structuring your paper.
Recommended Assignment Template
Abstract
1.0 Introduction
2.0 Experimental Description
3.0 Cure Kinetics and Rheology Calculations
4.0 Process Optimisation
5.0 Quality Control Testing
6.0 Conclusion
7.0 References
Your paper should be minimum of 2000 words (excluding references). It should not exceed 2500
words. Note: YO ...
This presentation will give insights in importance of ergonomics, and time and motion study in designing workplace and how an ergonomically designed workstation/workplace impacts on productivity of operators/workers.
This presentation gives suggestions with examples on how to evaluate workplace for lighter assembly works and how cycle time can be reduced for specific jobs
Modern Computing: Cloud, Distributed, & High Performanceinside-BigData.com
In this video, Dr. Umit Catalyurek from Georgia Institute of Technology presents: Modern Computing: Cloud, Distributed, & High Performance.
Ümit V. Çatalyürek is a Professor in the School of Computational Science and Engineering in the College of Computing at the Georgia Institute of Technology. He received his Ph.D. in 2000 from Bilkent University. He is a recipient of an NSF CAREER award and is the primary investigator of several awards from the Department of Energy, the National Institute of Health, and the National Science Foundation. He currently serves as an Associate Editor for Parallel Computing, and as an editorial board member for IEEE Transactions on Parallel and Distributed Computing, and the Journal of Parallel and Distributed Computing.
Learn more: http://www.bigdatau.org/data-science-seminars
Watch the video presentation: http://wp.me/p3RLHQ-ghU
Sign up for our insideHPC Newsletter: http://insidehpc.com/newsletter
Management of Library Automation
Library Automation refers to the use of computers to serve the needs of library users. The operations of a library get a quantum jump with the introductions of computers. The computers help to provide fast and reliable access to the resources available in the library as well as elsewhere. The application of computers in the library operations avoids repetitive jobs and saves lot of labour, time, speeds up operations, increases use of library resources. Computers are not only used as a tool for processing the data, but also for data storage and accessing. Planning for an automated system, no matter how big or small, should be part of an overall long-range plan for the library. Automation should always be used as a means to achieve overall better patron service.
Library Automation refers to the use of computers to serve the needs of library users. The operations of a library get a quantum jump with the introductions of computers. The computers help to provide fast and reliable access to the resources available in the library as well as elsewhere. The application of computers in the library operations avoids repetitive jobs and saves lot of labour, time, speeds up operations, increases use of library resources. Computers are not only used as a tool for processing the data, but also for data storage and accessing. Planning for an automated system, no matter how big or small, should be part of an overall long-range plan for the library. Automation should always be used as a means to achieve overall better patron service.
Curation-Friendly Tools for the Scientific Researcherbwestra
Presentation for Online Northwest Conference, in Corvallis Oregon, February 10, 2012.
Highlights electronic lab notebooks (ELN) and OMERO (Open Microscopy Environment) as two tools that enable researchers to better manage their research data.
Requirements engineering scenario based software requirement specificationWolfgang Kuchinke
Requirements Engineering – Writing the Software Requirements Specification (SRS). A CRI Group Workshop. The requirements engineering approach employed successfully in the EHR4CR process is shown and discussed in order to extract lessons learned and to use it for new projects.
Requirements engineering is the process of eliciting stakeholder needs and desires and develope them into an agreed set of detailed requirements. It serves as basis for all subsequent software development activities.
In general, a project begins with the requirement acquisition phase and ends with the specification of requirements in form of the Software Requirement Specification (SRS). Requirements specification may even be used to manage the consistency of the entire system.
Learning from the Requirements Engineering process in the the EU project EHR4CR. Especially the topics of Requirements Scenarios in the process of requirement gathering and the iterative writing and validation of software requirements specification (SRS) document can be applied to new projects. The Requirements Process consists of 4 steps: Requirements Elicitation – the art to receive meaningful requirements. Requirements Analysis – iterative improvement of quality of requirements. Writing the Requirements Specification document (Software Requirement Specification) and Requirements Validation - this is also done iteratively with several workshops.
Novel is the introduction of an iterative process for requirements engineering. Start with only a subset of software requirements, iterate the collection and validation until the full system is implemented. In each iteration, design modifications are made and new functional capabilities are added. Following tools for requirements gathering were used: Use Cases, Descriptions of current situation and workflow, Context diagram, Stakeholder interviews, Scenarios and Use Case workshops.
A novel scenario based approach for requirements engineering is being introduced: The domain scenario is used to estimate probable effects (situation analysis and long-range planning). The domain scenario is broken down into high-level "Usage Scenarios". Usage Scenarios describe critical business interactions and their anticipated operations; they serve as context for the use cases and the generation of requirements; they make sure requirements are complete.
Development of the SRS with involvement of scenarios: 1. Begin with Domain Scenarios; 2. Development of Usage Scenarios; 3. Software Requirements Specification document. Several round of change management were employed during writing the SRS. This possibility for correction and improvement ensured that the requirements are of high quality and applicability.
Diagnostic hypothesis refinement in reproducible workflows for advanced medic...Cezary Mazurek
(1) In-Silico experiments, especially in their refinement cycle, lead to creation of new software tools, algorithms and even computer science challenges. To make this experiment valuable such a process need to be controlled and recorded while achieving milestone stages;
(2) Scientific experiments are performed in cycles, when each cycle is a refinement of hypotheses. Continuing research starting from any cycle and branching this process further on, require that each cycle is checkpointed and stored as a scientific procedure step;
(3) Medical research reliant on data analysis, focused on early disease diagnosis or stopping the disease progress, very often results in providing software tools helping in data analysis and created during the experimentation cycles. To treat the process of knowledge discovery based on data analysis and development of processing tools, as a research method, we need to provide the way of formal description of stages of such a process, be paired with hypothesis refinement stages.
‐ Total Assessment Weighting ‐ 25 Introduction T.docxodiliagilby
‐ Total Assessment Weighting ‐ 25%
Introduction:
The optimisation of processing times is an important skill for all engineers and is often undertaken
via a modelling approach. The processing of composites can be a long process and a bottleneck in a
production line. The temperature profile during the composite cure can be adjusted to reduce
processing time and increase part output during production.
The quality control of composites is also time consuming and costly. Most non-destructive testing is
inconclusive, so thermal and mechanical testing is conducted to ensure quality is consistent.
Choosing the most cost and time effective method is critical to meet high standards in an efficient
way.
This assessment task is based on experimental work performed during Practical 1. You will be
creating a ‘technical research paper’ based on your composite experiments performed during week
2 and 3.
Assessment task:
In Practical 1 you performed a set of experiments related to optimizing the manufacture of
composites. Using the template provided, you will create a technical research paper based around
these three experiments. Please read the template carefully in terms of how to write and structure
your technical paper. Your paper will discuss the following elements.
1) Calculation of Kinetic and Rheology Constants: Using information in the literature and unit
content, use data generated from a Differential Scanning Calorimetry (DSC) and/or
Rheometer to find the constants to be used for the modelling of viscosity curves. A proposal
of potential alternative solutions to create a model for resin viscosity is to also be presented.
2) Optimisation of flow through a fibre stack: based on your observations from the practical
and from the experimental data collected, you will use the rheology model created to
optimise the temperature profile for increased flow of resin through a fibre stack, and
predict the time it will take to reach the tool surface and wet out the fibre tack surface.
3) Quality Control Testing: Recommend and justify a test procedure to measure the following
key properties of a manufactured component:
• Glass Transition Temperature
• Tensile modulus
• Internal porosity
• Bond between carbon fibre plies
• Degree of cure/conversion percentage
• Fatigue
• Fatigue at temperature
Discuss whether the recommended procedure is standardised, the data that needs to be
collected and calculations that need to be made.
Writing the Report:
You are welcome to use the recommended title template below as a guide to structuring your paper.
Recommended Assignment Template
Abstract
1.0 Introduction
2.0 Experimental Description
3.0 Cure Kinetics and Rheology Calculations
4.0 Process Optimisation
5.0 Quality Control Testing
6.0 Conclusion
7.0 References
Your paper should be minimum of 2000 words (excluding references). It should not exceed 2500
words. Note: YO ...
1. NB: Please note the term "Problem Statement." This assignment is to identify
and solve an HFE problem in your workplace. Follow standard quality
improvement problem-solving guidelines - which start with a well defined
problem.
If it looks like PDSA - you are probably close.
Sample from previous semester:
Title: Countermeasures for Pack Station Pains
Introduction & Problem Statement
Developing HFE countermeasures to alleviate human discomfort and efficiency in pack
stations within the warehouse.
Background
Brief history of general pack station set up
Basic requirements
A look around the globe
Analysis
Where are the pains?
EHS information in support of changes needed
Table
Location
Height
Depth
Equipment
Placement
Usage
Supplies
Placement
Storage
Availability
Product
Placement
Weight
Movement
Individual needs versus consistency of stations
Potential HFE Countermeasures
Manipulate pack station area
Determine suitable table configuration
Correct equipment placement for optimal usage
Enable quick availability for supplies
Promote proper handling of larger products
Conclusion
Clearly, there can be no conclusion as yet
2. Your final project paper will have a conclusion -- but as of now -- no jumping to
conclusions.
Page 1 – Title PageTopic / TITLE:
Mitigating Repetitive Motion Injury (RMI) on the wrist caused by a Fitting Driver
Page 3 – Introduction (Background / Problem Statement)
Description of the process in question or the affected process (Fitting Installation Process)
What are the detailed steps involved
How is the process considered an HFE issue
A specific description of how a fitting driver or the process become an HFE problem
Analysis (5Ms & E Approach):
Man: is the operator trained or qualified on performing fitting installation?
Machine: is the fitting driver ergonomically designed? Is it operator friendly?
Method: is the current fitting installation method optimized? Is there a written procedure on this process (work
instructions, standard operating procedures, etc.)?
Material: what are the materials involved in the process that can contribute to the problem?
Measurement: Is the fitting driver’s torque specification optimized? Is there a measurement system in place to
monitor fitting driver’s spinning torque?
Environment: is the work station lay-out/design optimized? (Table height, width, etc.) How do the issues in each
process components (5Ms & E) related or associated with RMI?
Possible HFE countermeasure or intervention:
Training, operator qualification/certification on performing fitting installation
Fitting driver design modification (fixtures, motor, etc.)
Job rotation of operators in a shift (currently: none; at least every 4 hours or even every hour)
Implement stretching exercises during or after breaks
Change work station lay-out (5S, etc.)
Create process work instructions that includes Dos & DONTs
Investigate on the possibility of lowering the fitting driver spin torque setting
JB
Page 1: Title Page
Preventing and alleviating neck discomforts and injuries from sustained microscope use
Page 2: Abstract:
Short summary of project and findings
Page 3-15: Body
Introduction:
o Discuss problem: Neck injures form sustained microscope use
o State why this is a HFE problem and how I plan on addressing the problem
o Discuss literature that supports the problem and connect to the problem at hand
o Talk about HFE approaches to fix and/or lesson the problem
Methods (may include diagrams and other visual aids)
o Environment:
o Body position in relation to microscope
o Table height
o Chair adjustability
o Work area
o Microscope
o functions
o adjustability
o lighting
o Other contributing laboratory equipment or tools
o Operator Brakes
o Are there enough/not enough brakes taken
3. o Stretches that counter sustained neck/body position from microscope use
o Countermeasures
o Actions taken to better HFE conditions
o Etc. (all other relevant information/actions)
Results
o summary of results from methods
o what relevant/irrelevant HFE changes were made
Discussion/conclusion
o HFE Findings/improvements to work environment
o Future improvements and perspectives
o Conclusion
Page 16: References
Cara
PRELIMINARY PLAN TO ATTACK THE FATIGUE OF THE COUNTERSINKING
OPERATORS.
PROBLEM STATEMENT
o Historically there have been complaints about the poor adaption of the tools and workstation for the task of
countersinking the assembly holes on the 171-181 doorgates. On top of that there is always an overload of parts to
be worked. The proposal is to help operators health and productivity via HFE improvement.
IDENTIFICATION OF VARIABLES THAT INFLUENCE THE PROBLEM.
o Methodology, Procedures, Documentation.
o Tool used, measurements.
o Environmental variables.
o Work load.
o Materials related issues.
o Operators factors, training, supervision.
POSSIBLE COUNTER MEASURES.
o TOOLS
o DOCUMENTS, INSTRUCTIONS, TRAINING
o WORKSTATIONS.
VERIFICATION AND CONCLUSIONS.
Becara
JC said: "Post your outline here."
TITLE:
Human Factors in Medical Record Storage
INTRODUCTION
Purpose of the project
(The need for record storage plan in preparation for implementation of electronic medical record (EMR))
PROBLEM STATEMENT:
Determine the most appropriate record storage format for current hard-copy patient records in preparation for an
electronic medical record
BACKGROUND:
• Definition and examples of medical records
• Requirements for retention of medical records
• Potential uses of stored medical records
• Storage methods
ANALYSIS:
PAPER RECORD STORAGE ASSESSMENT
• Amount of paper records currently stored
• Amount of paper records to be generated per month through
transition to EMR
• Reduction of paper records as they reach destruction dates
4. •
Shelving storage space required for paper record storage over next
10 years
• HFE evaluation of worker requirements to support paper record
storage
o Hours required to move records to overflow record storage
area
o Hours required to pull records for destruction
o Hours required to pull records on return patients (re-activated)
o Mechanics of pulling, storing, labeling boxes of records
(weights, heights of shelves, impact of lifting, injury potential,
etc.)
ASSESSMENT OF ELECTRONIC STORAGE OF PAPER RECORDS
• Amount of electronic storage space required to store current paper
records and additional paper records over next 10 years
• HFE evaluation of worker requirements to support scanning paper
records into electronic format:
o Process and equipment required to scan paper documents,
including quality control for accuracy and readability
o Mechanics of scanning documents (standing positions, lifting,
twisting, etc.)
o Workstation design for scanning
o Hours required to scan current volume of paper records
o Hours required to scan additional records over next 10 years
o Hours required to reproduce records upon readmission or
subpoena
POTENTIAL HFE COUNTERMEASURES:
• Procedures that require less human interaction with stored paper
records
• Alternative storage options, such as outsourced storage services
• Scanning equipment that is faster, easier, efficient for the worker
CONCLUSION:
Identification of solution that is safest for the workers and cost-effective for the facility.
Robin
rofessor JC wrote: "Post your outline here."
TITLE: The Use of Human Factor Engineering to Improve Laboratory Layout.
INTRODUCTION/PROBLEM STATEMENT:
Laboratory space is limited; however, working conditions can improve greatly by utilizing the space provided. With
multiple people using the same equipment, rearranging the lab to "work stations" will not only greatly improve the
use of the space; but also, improve the time needed to perform each task. One aspect of this project, is to prevent
additional risk for those who are performing a test with the unnecessary need to walk to the other side of the lab to
complete a test.
BACKGROUND:
o Give a history of the lab being used.
o Explain the current work environment.
o Current culture
o Explain the concerns of current lab personnel.
o Explain the tests involved.
o Explain the need for the change.
ANALYSIS:
o Possible areas of pain.
o Current location of equipment.
o Possible hazard of current work stations.
5. o Current location of chemical storage.
o Possible hazards of current chemical storage.
o Lack of movement/space when all lab personnel are in the lab.
o Time needed to perform tasks.
POTENTIAL HFE COUNTERMEASURES:
o Relocation of workstations.
o Difference layout of workstations.
o The addition of workstations (if room permits).
o Advanced equipment (if budget permits)
o Reorganization of lab drawers around workstations.
o Relocation of chemicals used for easier access.
CONCLUSION:
TBD – Hopefully, very happy lab personnel!
1- Title: "HFE accessorize and tools to reduce manual handling in the laborator
2- Introduction & Problem Statement
Manual handling involves any activity that requires the use of force exerted by a person to lift, lower, push, pull,
carry, move or hold an object
In the laboratory many repetitive actions and practices, most notably, pipetting., weighing, diluting solutions,
processing data, microscopy, and solvent transferring from one place to another, all these activities .are classified as
manual handling.
These activities have the potential to cause muscle strain and pain in the lower back, the fingers, the hands, the
shoulders, and even the arm and the legs
3- Analysis
•&νβσπ; Analyse the traditional practices during performing different activities like pipetting. weighing, diluting
solution, processing data, microscopy, and solvent transferring from one place to another and study the he negative
effects on the human body.
4- Potential HFE Countermeasures
•&νβσπ;Find out the proper and the safe way to handle these activities and the HFE role in improving these
practices.
•&νβσπ;Compare cases before and after implementing the HFE
•&νβσπ;What does it cost to implement the HFE measurement in the laboratory
•&νβσπ;
5-Conclusion
6-References
7-Glossary
8-Album
Wissam
Dr. JC wrote: "Post your outline here."
Title
Prevent nonconforming empty packages from escaping the visual inspection process
during clean room packaging.
Abstract
Summary of the project, and brief description of results.
Introduction & Problem Statement
Utilize HFE tools to minimize empty packages escaping the visual inspection process
during clean room packaging.
6. Background
ü Introduction to laboratory tools packaging station set up
ü Inspection procedure
ü Negative trending of Material Rejection Notice (MRN) due to missing components
Analysis
Cause and Effect Analysis (Fishbone Diagram)
ü Man: Is the operator trained on the Standard Operation Procedure (SOP) for Packaging?
ü Machine: Are there any common causes of variation due to machine design?
ü Method: Is the process validated and documented properly?
ü Material: Do the packaging components contribute to the production nonconformance?
ü Measurement: Is there a monitoring system to check for missing component?
ü Environment: Is the packaging station set-up properly? Does the clean-room
environment contribute to the packaging nonconformance?
Use the 5 Whys technique
ü get to the root causes of the packaging nonconformance
Possible HFE countermeasure:
ü Check training records for packaging personnel
ü Belco Machine (package sealing machine) modification
ü Consider flextime, compress time arrangements
ü Introduce eye exercises during inspection
ü Remodel packaging inspection station
ü Revise SOP, add workmanship standards with pictures of nonconforming packages
ü Drive our fear of manager retaliation
Data and Results:
ü Data collected will be summarized and results will be posted in the conclusion
Conclusion:
ü Work in progress
Regards!
Guillermo
Sally Myer
HFE Project Paper Title: Use of Human Factor Engineering (HFE) to Reduce Medication Administration Errors by
Nurses
I. INTRODUCTION--EXPLAIN THE PROBLEM
A. Safety in healthcare
B. Frequency and types of medication administration errors
at my workplace
II. ANALYSIS OF ERRORS
A. Identification of Most Frequent Root Causes
1. Interruptions and distractions
2. Lack of cues when doses are due
3. Lack of standard medication administration process
III. POTENTIAL COUNTERMEASURES--UTILIZATION OF HFE
A. Strategies
1. Standardization
7. a. Standard Work
2. Visual Management
a. Communication Board
b. Electronic Status Board
3. Electronic Bedside Medication Verification (BMV)
a. Bar Coding
B. Tools/techniques to support adoption of countermeasures
1. Just Culture
a. Fair Management of Staff Behavior
2. Staff Engagement
IV. CONCLUSION