Review of clinical protocols and Case Report Forms (CRFs/eCRFs)
CRF and eCRF design, printing/deployment, distribution
Database design and development
SOP development
Data receipt, logging, and tracking
Data entry
Double data entry and cleaning/clarification
Data validation (manual check, computerized edit checks, medical expertise)
Data presentation in a format and structure convenient for the client
Electronic data transfer/handling
Biostatistics
Study design consultation
Study protocol development
Statistical analysis
Electronic Data Capture (EDC) implementation and site training and support
Study reports
Assistance in preparation of study results presentation.
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We invite you to consider our services and to contact us to discuss your clinical trial and pharmaceutical needs.
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