
Getting and Staying ePI-Compliant
On-Demand
Docuvera is a globally recognized leader in structured content authoring solutions for the pharmaceutical industry. Headquartered in New Zealand, Docuvera solutions have been implemented world-wide for more than a decade to strengthen regulatory compliance and governance as well as significantly improve content standardization/reuse efficiency and approval submissions/time to market. The company’s embedding of its proprietary artificial intelligence (AI) into the solution has further fortified the Docuvera as a soughtafter solution for pharmaceutical documentation use cases as well as a platform for customers to further digital transformation initiatives.
In this webinar, you will see how the Docuvera solution both facilitates and simplifies digital transformation, including the ability to generate ePI-ready submissions without coding expertise to downstream digital platforms like EXTEDO. Attendees will learn how to meet evolving regulatory requirements while preserving the ability to export traditional formats for downstream use.
The faster & safer path to global ePI compliance. Learn how Docuvera delivers the best of both worlds—ePI-ready submissions and traditional format export. Register now!
- Creating ePI using FHIR standards
- Portal-based eSubmission workflows
- Integrating health authority feedback
- Using mutable structured content to meet evolving regulatory needs
- Kenneth Gutierrez, MBA
Senior Product Manager, Docuvera
- Susie Winn
Director, Life Sciences Solutions, Docuvera
Who Should Attend?
- Regulatory Affairs Managers
- Global Product Labeling Owners
- Regulatory Technical Authors
- IT Professionals Supporting Regulatory Affairs
- Regulatory Compliance Managers