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 Application 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
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