Program by Day
Program by Track
Program Titles
A Comparison of Three Visual Help Authoring Tools
A Practical Guide to Capturing, Organizing, and Securing Your Documents
Being Smart About Global vs. Local During Clinical Trials
Bringing User Experience to Medical Devices
Centralized Translation Processes
Changes to Labeling Requirements for Pharmaceutical and Medical Equipment Professionals
Creating and Serving Relevant Content
Creativity or Confusion Factor?
Developing a Collaborative Team
Developing a Unified Enterprise Content Model
Drowning in a Sea of Information Whats Your Rescue Plan?
Globalization Issues with Medical Device Embedded Systems
Handling DITA Topics and Translation in a Regulated Industry
How to Enforce Standards in Life Sciences Documentation
How to Maximize Content for a Global Audience
How To Select and Procure Content Technologies
Marketing in a Connected World
Migrating to Structured Authoring on Your Way To XML
Phase 2 - What’s Next for Life Sciences and Enterprise Content Management
Preparing Compliant eCTD Submissions
Structured Content Beyond the Label
Structured Product Labeling Workshop
The Best Global Medical and Pharmaceutical Web Sites (and Why)
Transforming Technology Transfer and Recipe Management
Unlocking Handwritten Information from Medical Records
What’s New in Collaboration Tools
Writing Reusable Content for Different Audiences
XML-Based Collaboration with Office 2007
Your Global Audience is Already Here
[Case Study] Physician, Know Thy User
[Workshop] Analyzing Your Deliverables
[Workshop] Content Modeling for Life Sciences Content
[Workshop] Creating High Quality Content that Communicates Across Language Barriers
[Workshop] Do you Know Adobe Acrobat?
[Workshop] Games To Explain Human Capability and Limitations
[Workshop] Learning DITA From Concept to Implementation
[Workshop] Product Life Cycles in the Life Sciences Industry
Session Details
[Workshop] Games To Explain Human Capability and Limitations: A Fun Learning Experience For Life Sciences, Medical and Technical Writers
Speaker: Dr. Ronald G. ShapiroTime: 8:00 AM - 12:00 PM Date: June 26
Track: Post-Conference Workshops
Experience level: All levels
Medical error, which leads to patient discomfort, extended hospital stays, and sometimes death is often caused by problems in the design of the medical system and/or procedure. These design errors may lead to an incorrect action by medical personnel actively involved in patient treatment. For example a display may be overcrowded or too small. There may be too many like-sounding alarms of varying importance going off at once, so that the most important ones are missed. It may be very easy to set some equipment to administer medicine too quickly or too slowly. It may be possible to connect different types of tubing together which should not be connected to each other. All of these errors should be prevented by better design. This prevention requires knowledge of human capabilities and limitations by the people designing and producing the medical equipment and procedures.
The technical or medical writer on a product, process or solution development team, who knows about human capabilities and limitations can predict the errors which are likely to happen in the course of their job. The writer has less ego-involvement in the product design than the engineers. With some training they might also have more knowledge about human capability and limitation. Thus, they have the potential to become a critical team member who detects potential medical errors while reviewing designs and prototypes of products and procedures and suggests alternative designs that will ultimately save patient lives. Additionally, by making the equipment safer they may prevent costly recalls and law suits.
In this session we will perform a series of activities involving attending to details, communicating, conforming, responding, and transferring learning from one environment to another. These activities show what people can do very well and where they are prone to sub-optimal performance. We will discuss some potential implications of these human strengths and weaknesses for the design of medical equipment and procedures so that the technical writer will become more equipped to help make their products safer, faster, and easier to use. In addition, the activities will illustrate some principles which may help to improve the design of documentation.
This session is a great way to conclude your formal conference participation because it is informative, interactive, fun, and a great initial step towards learning about preventing medical error and saving lives. You might even win a prize and learn a few parenting skills, too!!!


