The DITA Pharmaceutical Content Subcommittee will define DITA topics, maps, associated metadata properties and terminology to streamline design and creation of the complete body of pharmaceutical documentation required to present a product for scientific and regulatory purposes throughout its lifecycle.
These constructs will include a pharmaceutical content taxonomy of DITA topics, the metadata and terminology to be associated with each topic instance, and a taxonomy of DITA maps--all of which will be defined to optimize reuse and re-purposed content.
The group will initially focus on defining topics and maps as required to implement:
- ICH Common Technical Document content specification
- FDA Structured Product Labeling
- EU Product Information Management content specifications
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