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Getting and Staying ePI-Compliant

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

概览

This On-Demand 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.


精选主题

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

谁应该参加?

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

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