CRF개발 및 가이드라인 작성부터 임상시험 완료 후 DM 및 통계까지  제공하며, 임상시험계획서 및 표준작업지침서 (SOP)를 준수하여 Data Management 및 Statistical Analysis의 계획, 분석 결과를 제공합니다. 

We provide services such as CRF development, guideline set-up, DM and statistical anaylsis after clinical trial; and also provide Data Management and Statistical Analysis planning and analysis result that comply with clinical trial protocol and Standard Operating Procedure(SOP).

▶   Data Management Plan (DMP)
▶  CRF Development
▶   Data Validation Specification (DVS)
▶   Database Buildup and Validation
▶   Query Management
▶   Medical coding
▶   Database Quality Check
▶   Database Lock

▶   Sample size Calculation
▶   Randomization Management
▶   Statistical Analysis Plans
▶   Statistical Analysis Reports