Global regulatory requirements are rapidly increasing in complexity, making it harder than ever to maintain compliance across your product portfolio. Join our regulatory expert to get ahead of upcoming changes that will impact your operations in 2025 and beyond.

We’ll provide a practical roadmap for navigating critical regulations including eCTD, IDMP/SPOR, EUDAMED/UDI, and ePI requirements. Get actionable insights on how industry leaders are transforming their operations to ensure consistent compliance in an increasingly complex regulatory environment.

Moderator:

Agnes Cwienczek
Director of Product Management, ArisGlobal

Key topics include:

  • Deep dive into upcoming regulations and industry trends
  • Critical regulatory changes coming in 2025 and beyond
  • Practical strategies to prepare your operations
  • Best practices and guidance from industry leaders

*All registrants will receive the on-demand recording.

Don’t miss this opportunity to gain:

  • Expert insights on emerging regulatory requirements
  • Practical strategies for maintaining consistent compliance
  • Best practices for navigating complex global regulations
  • Live Q&A with our regulatory expert 

Why attend an ArisGlobal regulatory webinar: 

  • 35+ years of expertise serving the life sciences industry
  • Trusted by 300+ global life sciences organizations
  • Deep domain knowledge of evolving regulatory frameworks
  • Proven solutions that enable consistent compliance