Clinical data management


(e)CRF design
Database setup and maintenance
CRF tracking and status reporting
Data entry
External data integration (e.g. central lab data, ECG data)
Data validation and query management
Medical review
Serious Adverse Events (SAE) reconciliation
Coding (e.g. MedDRA, WHO-Drug Dictionary)
Database transfer



News and Events

eClinical Solutions
with Real-time, Risk&Workflow Management:


An integrated Artificial Intelligence Platform for Study Control – KOEHLER eClinical´s VITESSA Trial Control System (TCS)
Meeting:
DIA Europe 2019 Vienna 05-07.02.2019
Speaker:
Dr. Manfred Koehler, CEO, KOEHLER eClinical GmbH

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