OASIS invites participation in new DITA Pharmaceutical Content Subcommittee

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
OASIS welcomes participation in the DITA Pharmaceutical Content Subcommittee by all interested parties. Contact communications@oasis-open.org for more details.



Reference links

XML.org Focus Areas: BPEL | DITA | ebXML | IDtrust | OpenDocument | SAML | UBL | UDDI
OASIS sites: OASIS | Cover Pages | XML.org | AMQP | CGM Open | eGov | Emergency | IDtrust | LegalXML | Open CSA | OSLC | WS-I