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Non-Commercial Clinical Trials

Non-Commercial Clinical Trials

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Services in Clinical Trials

Support in writing a funding application 

Start-up – initial and subsequent submissions, budget and contract negotiation 

Monitoring and site visits – selection, initiation, monitoring, close-out, booster 

Creating study documentation and templates

Creation of source documentation forms („worksheets”) 

eCRF, ePRO, data management 

Preparation  „Investigator Site File” 

Management of payments to investigators and healthy volunteers 

Patients travel reimbursement, cashless transport of patients to the site for the visits

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