Clinical Study Management

Clinical Study Management enables the business to gather required essential documents to achieve study site initiation readiness accurately and quickly, across the globe.

Clinical Study Start Up made easy

One of the key challenges facing any global pharmaceutical company is keeping up with and adapting to the amount of change and variation in regulatory requirements around the world. The Clinical Study Management application, provides an automatic way to generate the right list of documents required for a local site anywhere in the world. It also features a process to manage change to those rules easily as necessary, via business rules that drive the essential document lists from a business friendly user experience.

Clinical studies are a precursor to clinical trials and ultimately, new drug introductions. While the volume of on-going studies is relatively low, they span long periods of time, involve numerous documents and participants, and span multiple locations in many countries. CSM achieves study site initiation readiness accurately and more quickly than ever before, by increased process visibility, speed to start-up and accurate country-level documentation - which were all former pain points, with clinical studies.

Key Highlights

Intuitive workflow that brings information to the user as they need it
Establishes Appian as the integration point from multiple external systems, and making the data actionable though related actions
Increased performance visibility through executive dashboards
Actionable reports that highlight missing or at risk items

Clinical Study Management in action

Clinical Study Solution on Appian AppMarket

Princeton Blue’s Clinical Study Management solution has been approved by Appian and is listed on the Appian AppMarket.

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