Cytestream brings a holistic, unconventional approach to address a key aspect of drug development: clinical sites and trials.

This CFR Part 11 compliant, cloud-based software manages all aspects of trial operations: from planning and study start-up to closing. Ideal for independent study sites and networks, it empowers both trial sites and sponsors to conduct quick, accurate, and process-compliant research.

Users

CROs, bio-pharma sponsors, and trial sites – Cytestream addresses your unique challenges to speed-up clinical studies.

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Benefits

Improved visibility, communication, and compliance. Faster and accurate procedures. Cytestream builds efficiency across clinical trial processes.

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Features

Patient database management, quick document sharing, reporting, and financial tracking – all that you need to simplify trial management.

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