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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 technologies. 

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 advice.

If You want to know more please contact us.