ClinConcept supports Pharmaceutical Companies, Biotechs and CROs with adopting new technologies
and processes for Clinical Trials in the area of EDC (Risk based Monitoring), Patient Reported Outcomes and Document Management.
We help our customers to clearly
define and document requirements, find the right modality for
their specific protocol, select and manage technology vendors and
project manage the technology part of their trial.
In addition to this we support the implementation of Data Standards (e.g., CDISC) and adjusting SOPs to maximize the Return on Investment into new
With more than 20 years of experience in Clinical Research
working for CROs, Sponsors and technology companies we have a broad
understanding of the available technology and provide vendor neutral
If You want to know more please contact us.