Streamline Operations with Unified Regulatory Information Management

Duration: 60 minutes


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Why watch


Join this webinar co-hosted by Veeva and PharmaLex to learn how a unified RIM solution can help companies streamline regulatory processes and make those partnerships more effective and powerful. We’ll focus on high quality document and data standards, worldwide accessible systems, and efficient processes for capturing and managing information in a seamless and secure manner across different sources. In addition, we’ll share a case study from Alnylam and our best practices for delivering high-quality, impactful implementations with an emphasis on measuring success in the short and long term.

Key Learnings

  •  How Alnylam optimized their regulatory processes and technology to support expansion into new markets
  •  Best practices for delivering a high quality and impactful RIM implementation with an emphasis on measuring short and long term success
  •  How to capture and manage regulatory information semalessly and securely across different sources
  •  Effective strategies for managing global document and data standards

A full day of inspirational speakers

Proud to bring inspirational speakers from across the globe. 

Katrin Spaepen

Director Strategy Vault RIM


Jennie May

Director Regulatory Operations, PharmaLex

Katrin Spaepen

Director Strategy Vault RIM


Timm Pauli

Head of Global Regulatory Informatics and Operations, PharmaLex