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 learning objectives:
- 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
