Key Concept Archive

For more information about how our library science background (and our love of all things metadata) guides the way we catalog information, see the Techcomm and Arbortext Resources page.

XML Saves Lives

I know it sounds dramatic, but it’s not hyperbole. If your business is regulated or has strict standards applied, XML is critical and quickly becomes a strategic advantage! XML gives you several advantages over desktop publishing that can help address…

Collisions in Patient Education: Surveillance, Medical Devices, and Communication

Room 42 is where practitioners and academics meet to share knowledge about breaking research. In this episode, Krista Kennedy and Noah Wilson, Syracuse University, discuss the complexities of algorithmic ecologies in medical wearables and navigating data surveillance disclosure in patient…

Structured and Unstructured Content: Perspectives from a Data Governance/Privacy Analyst

In this presentation, attendees will take a high-level drive through the world of Data Governance from the eyes of a new Data Governance/Privacy Analyst. We’ll review the Data Governance Lifecycle, the three data content stages (structured-unstructured-semi-structured), the four data classifications….

Teaching Martians to make a sandwich–How Technical Writers can improve patient safety

There’s a well-known exercise to experienced technical writers: How do you teach a Martian to make a sandwich. It’s so well known that we talk about it as an exercise in best practices for user experience and modern instructional design….

What happens when you skimp on documentation?

In the TC Dojo last week we found out: Your company is at risk of debilitating lawsuits that, in the worst case, can put you out of business. Joe Devney, forensic linguist, editor, non-fiction writer, and previous STC chapter chair shared…

Manage your product content like you manage development

Meet compliance and regulatory challenges Medical device manufacturers are facing some very tough challenges today including demand for innovation, complying with strict environmental and regulatory requirements, and shrinking price premiums, not to mention intense competition which demands faster times-to-market. The…

Documentation, Medical Devices, and the FDA

This month the implementation date for MDD directive (2007/47/EC) comes due. There are a number of issues that require action by manufacturers (changes to the Essential Requirements, clearer requirements for clinical evaluation, changes to the QA of third parties) and…

Dynamic product information delivery systems reduce translation costs

Recently, I was privileged to talk with a customer that implemented Arbortext in 1999: Greg Johnson at Medtronic. Greg heads up what his executives have told him is “the most successful project Medtronic had ever done.”  In this interview, Greg…