by Anders Vesterberg | Thu, Nov, 2019 | Structured Content Series
In the pharmaceutical industry, the high volume of documentation necessitates precise and accessible analysis, control, and tracking. This can be accomplished with intelligent metadata. Metadata provides human-readable summaries and machine-readable information about...
by Lisa Sookraj | Wed, Sep, 2019 | Structured Content Series
Pharma companies face unique challenges when submitting product labeling to regulatory bodies. One such challenge is managing complex document relationships and associated processes throughout the submission lifecycle. Clearly defined document relationships ensure...
by Anders Vesterberg | Wed, Jul, 2019 | Structured Content Series
It’s no secret that the manufacture of pharmaceuticals requires extensive documentation. Keeping this documentation consistent and compliant across jurisdictions can be time consuming and error-prone, which may delay a drug’s time to market. Structuring the content...
