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Safety Case Study


A large multinational medical device and health care organization embraces ArisGlobal’s LifeSphere LitPro to effectively automate all steps in the medical literature monitoring process.

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The client, a mid-tier biotechnology company with products in a range of therapeutic areas, was struggling with an all-too-familiar challenge: How to effectively collect, organize, triage and archive the large volume of inbound potential AE (Adverse Event) and ADR (Adverse Drug Reaction) reports they received for case processing and reporting.

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