Meeting the challenge of optimized, most efficient use of regulatory information can be a complex and challenging process throughout the product lifecycle—whether your primary focus is either business or technology.

To support continuous learning, DIA brings you complimentary digital downloads to spur thought, reflection, collaboration, and action. In your Resource Kit, you'll find links to intriguing articles, exclusive podcast interviews, session recordings from DIA events, and more!

Introducing our NEW Regulatory Submissions, Information, and Document Management Forum eBook! Filled with even more resources, global updates, forum highlights, track descriptions, and more, this eBook will help you in your day-to-day as well as prepare you for the forum in February!

  • How Continuous Publishing Speeds Regulatory Submissions
  • On-Demand Webinar: The Challenges of eCTD Implementation in Small Company and Academic Settings
  • Optimizing the Use of Electronic Data Sources in Clinical Trials: The Technology Landscape
  • Podcast: Regulatory Landscape of Drug-Device Combination Products
Download Kit