Regulatory Information Management Systems/Software, or RIMS platforms have emerged to assist pharmaceutical companies in submitting products for regulatory review. 

In this case study, we discuss how a global pharma company benefitted from Astrix’s expertise to:

• Define business processes to transition to Veeva’s RIM Solution.
• Develop Use Cases to drive configuration sessions.
• Define Release Plans to support implementation of Labeling capabilities.
• Efficiently track configuration items, and enhancements, and produce a summary of findings.

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