Already a DIA Member? Sign in. Not a member? Join.

Sign in

Forgot User ID? or Forgot Password?

Not a Member?

Create Account and Join

Virtual

Jun 04, 2025 12:00 PM - Jun 04, 2025 1:00 PM

(US Eastern Standard Time)

Getting and Staying ePI-Compliant

Learn how Docuvera delivers the best of both worlds—ePI-ready submissions and traditional format export.

Overview

This Solution Provider Webinar is brought to you by DIA in cooperation with


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 sought-after solution for pharmaceutical documentation use cases as well as a platform for customers to further digital transformation initiatives.


Featured topics

  • Creating ePI using FHIR standards
  • Portal-based eSubmission workflows
  • Integrating health authority feedback
  • Using mutable structured content to meet evolving regulatory needs

Who should attend?

Professionals who work in the area of:

  • Regulatory Affairs Managers
  • Global Product Labeling Owners
  • Regulatory Technical Authors
  • IT Professionals Supporting Regulatory Affairs
  • Regulatory Compliance Managers

Have an account?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.