As Structured Product Labeling (SPL) continues to evolve and become adopted throughout the FDA, organizations must ensure their original approach to SPL compliance is the best strategic fit for the enterprise. Initially, the goal for most organizations was focused solely on implementing systems and/or processes to achieve SPL compliance. Depending on your approach, SPL compliance can either result in additional time and cost to the overall submission process, or provide long-term value across the enterprise.
With additional XML-based standards under development, and the ability for structured content to drive efficiencies throughout an enterprise, it is prudent to review your overall approach to structured content authoring and publishing. This presentation looks at how XML can be used to manage content for SPL submissions to the FDA, Product Information Management (PIM) submissions to EMEA, as well as other uses such as standard response letters for customer contact centers.
SPL & Beyond: XML in the Life Sciences was presented by Don Bridges & Joe Jenkins, Commercial Technical Documents Manager, Data Conversion Laboratory (DCL) & Life Sciences Market Director, RWD Technologies and aired on 2006-04-06. For more details, or to download this conference, please visit our site at www.fxconferences.com
