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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?
Extending Your Reach with SMS (Text Messaging)
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
Reducing Multinational Product Launch Times and Localization Costs
Structured Content Beyond the Label
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
[Workshop] Simplified Technical English
Session Details
Handling DITA Topics and Translation in a Regulated Industry
Speaker: Jennifer Linton & Jennifer PerkinsTime: 2:00 PM - 3:00 PM Date: June 25
Track: Localization & Translation
Experience level: All levels
Room: B & O
Gambro BCT, a medical device manufacturer, is diving in to the next generation of technical communications. This new environment consists of topic-based XML/DITA-structured authoring, automatic publishing, and the need increase the number of language offerings to support growth in additional and merging markets. All of this is to be done while continuing to follow regulatory guidelines.
In this discussion, Jennifer Perkins, the Technical Communications Manager, and Jennifer Linton, the XML/CMS Project Manager, provide helpful tips about each phase of the document lifecycle and what to consider when moving to an XML/DITA-based environment in a regulated industry. Do you have questions about how to support an XML/DITA-based and content and translation management system environment in your industry? This talk will provide you with some helpful tools and answers for you to move forward.
After about two and a half years of attempting to move to DITA and trying different content management system approaches, Gambro BCT is finally using the open source authoring standard, a content management system, and a translation management system. This new environment, called GEM (Globalization and English Management), is the basis for many new opportunities at Gambro BCT. They will share a brief overview of the organizational structure, tools infrastructure, and the regulatory standards needed to maintain this new environment. Then they will dive into some of the details about the discussions they had to solidify this working environment. These discussions include the information model, user guide for the content management system, persona descriptions, and process and procedure guides. For example, in their discussions, they determined that the document lifecycle needed to change to encourage regulatory signoff at a more granular level to promote a translations cost savings.
The presenters will also share the benefits that they foresee with this new environment as well as some lessons learned and next steps, including implementation of this system to develop training materials.



