DXC Publisher, a scalable solution that can be implemented on premises or in a cloud environment, can simplify the submission process.
With a one-stop-shop approach, Publisher gives life sciences companies a user-friendly tool to manage regulatory submission documents in multiple countries. What sets Publisher apart is its use of templates, which eliminates the duplication of selections and settings. Regulatory agencies in different countries and regions can be targeted at the same time from a single publication template.
With the global nature of today’s pharmaceutical industry, life sciences companies must prepare multiple submissions that meet a wide variety of regulatory requirements. DXC Publisher, a scalable solution that can be implemented on premises or in a cloud environment, can simplify this challenging process.
As the most powerful submission tool on the market, Publisher helps companies meet region- and country-specific requirements and increase speed and efficiency. The solution covers the full gamut of worldwide regulatory submissions. It helps organizations build, review, publish and validate paper common technical documents (CTDs), non-eCTD electronic submissions (NeeS), legacy/rest-of-world submissions, clinical study reports and other generic reports. The solution offers flexible structures for document creation and works seamlessly with the DXC Regulatory Business Automation Software portfolio.
DXC Publisher — Simplifying regulatory submissions:
- Simplifies complex regulatory processes
- Increases speed and efficiency of regulatory submissions
- Shortens submission cycles with automation
- Builds intuitive submissions in a number of different formats
- Easily generates tables of contents, tables and figures
- Lowers development costs by reducing validation time
