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Virtual

How Leading Global Pharma Embraces AI to Automate Regulatory and Medical Documents with Quality Control

Join top-10 global pharma, AlphaLife Sciences, and Microsoft for exclusive insights and live demos on AI-powered document authoring—watch today!

Perspectiva general

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


AlphaLife


This webinar offers a rare, high-value opportunity for audiences to hear directly from top-10 global pharma, AlphaLife Sciences as the solution enabler, and Microsoft on the future of AI in regulatory and medical authoring. The session features Microsoft’s perspective on harnessing AI to reclaim time for scientific thinking, enable knowledge mining, and accelerate discovery. Attendees will experience enterprise-grade, agentic AI solutions, including auto-templating and scalable workflows that cover the full spectrum of document types such as ICF, Protocol, SAP, CSR, DSUR/PBRER, and CTD Module 2.7.x. A live demo will showcase end-to-end document automation with built-in QC in Microsoft Word and Veeva RIM, complemented by agent-based platforms for enterprise customization.

The panel discussion brings together pharma experts to share practical insights on business value, adoption challenges, solution requirements, and change-management practices for AI at scale, giving you direct insight into what’s working and how to accelerate your own roadmap confidently

Temas destacados

  • Microsoft perspective: AI in pharma—reclaim time for scientific thinking, enable knowledge mining, and accelerate discovery
  • Enterprise-grade scalable solutions: auto-template via agentic AI, supporting scalability across all document types, including ICF, Protocol, SAP, CSR, DSUR/PBRER, CTD Module 2.7.x, and more
  • Agentic AI platform for developers: AI agent-based workflows enabling enterprise-customized documents and workflows
  • End-to-end document automation software demo: regulatory and medical authoring with built-in QC—directly in Microsoft Word and Veeva RIM
  • Panel with top pharma: proven business value, enterprise barriers to adoption, solution requirements for regulatory documentation, and change-management practices for scale

¿Quiénes deben asistir?

Professionals involved in:

  • Drug R&D Leaders
  • Clinical Development Leaders
  • Regulatory Affairs Professionals
  • Medical Writers and Leaders
  • Regulatory Technical Authors
  • Labeling Professionals
  • Regulatory Compliance Professionals
  • Medical Affairs Professionals
  • Clinical Safety/Pharmacovigilance Experts
  • AI / Digital Innovation Leaders
  • IT Professionals

¿Tiene una cuenta?

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