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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] Product Life Cycles in the Life Sciences Industry: FAQ for the Vendor Selection Process

Speaker: Tina Cargile
Time: 1:30 PM - 5:00 PM   Date: June 26
Track: Post-Conference Workshops

Experience level: All levels

Life Sciences companies are not alone in their need to carefully consider linguistic and cultural issues as part of their global strategy, but the highly regulated nature of the industry does result in some unique aspects of the problem. In particular, these issues run the gamut of the product life cycle from product development, through clinical trials to eventual product release and marketing. Since these various activities are distributed among functional units in the typical life sciences company, the outside “language services provider” (LSP) sometimes has a better grasp on the “big picture” than any of the buy-side participants. Even in cases where there is centralized procurement of language services, the different linguistic requirements pertaining to different phases of the product life cycle may not be fully appreciated. 

This workshop will cover a multitude of frequently asked questions designed to help you use the vendor selection process to meet the variety of linguistic needs through the product life cycle and will include viewpoints of both the buyer and seller, with time included for participant Q&A. We will present a framework for understanding the scope of the vendor selection process, identifying opportunities to formalize or improve existing processes, and for leveraging technology at various stages of the product life-cycle. We will also suggest approaches to getting the most value from your LSP partner(s).