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Program Titles

A Comparison of Three Visual Help Authoring Tools

A Practical Guide to Capturing, Organizing, and Securing Your Documents

Authoring Assistance

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

Collaboration Via Reuse

Content Technologies Market

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… What’s Your Rescue Plan?

Ensuring Information Quality

Globalization Issues with Medical Device Embedded Systems

Handling DITA Topics and Translation in a Regulated Industry

Health Information Portals

Healthcare and the Internet

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

SPL Beyond CDER

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

Web 2.0 and Healthcare

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] Adobe Captivate

[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

[Workshop] Simplified Technical English

[Workshop] Writing Reusable Content

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. Shapiro
Time: 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!!!