Leave your study data to PHARMALOG, an expert in the efficient use of resources and services in clinical studies.
As our routes are short, we can immediately process the incoming data in our database system, which is validated in accordance with GAMP 5 requirements.
Thomas Huber (Head of Data Management) - his 30 years of professional experience mean that, with us, your data is in the safest hands.
If data are entered via an e-CRF system, we will be happy to provide you with validated EDC systems.
We will of course also treat data collected via paper CRF with the utmost care.
PHARMALOG also provides full data management support for your study. On request, we can provide you with the data in CDISC SDTM and CDISC ADAM format.