Optimising post-approval research: using technology for efficient and cost-effective studies

A large global Pharma company was required to run a complex global safety study by regulatory authorities. This was a crucial study to ensure that patients were not exposed to risk.

Cisiv was able to build a study in 10 weeks and launch it across 21 countries. Cisiv’s platform – Baseline Plus – was able to deal with complex data capture, analysis and reporting to various licensing authorities.

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