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Data Management

We provide sponsors, investigators, and patients with a comprehensive, end-to-end solution for the collection and management of all clinical trial data. In the case of both patients and sites, data will be effectively managed from the earliest stages of planning through study conduct and close-out.

Our experience includes eCRF build from our database (DB) builders on several preferred eDC tools. With this, we can find the perfect fit for your specific study and benefit from an agile and fast DB set-up.

We also offer other e-solutions in-house such as ePRO and eConsent, and we can reconcile and integrate data from a wide variety of sources.

How can we help you?

Contact our expert team to discover how Astrum can bring value to your clinical development projects.


Other services

  • Clinical Development & Scientific Advice

    Ranging from first in human to post-marketing, Astrum’s clinical development expertise spans the entire development cycle, 
offering support every step of the way

  • Biostatistics & Programming

    Through state-of-the-art implementation, smart design, and statistical methodology, your study will be optimised for sample size, duration, 
and population

  • Medical Writing

    We can flexibly support you from protocol to Clinical Study Report (CSR) writing. Across in-house clinical, regulatory, statistics, and medical colleagues, we’ll help achieve your study goals