Clinical Data Management (CDM) is a critical phase in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials.
StatRAC team can help you with:
Study Set-Up and Planning Activities
- Database design
- Configure web databases
- Create data entry forms
- Validation controls setup
Study conduct
- Data entry
- Medical coding using MedDRA and WHO
- Data validation
- CRF / eCRF tracking and annotation dictionaries
Database lock
- Merge randomization code to assign treatment groups
- Flag database records as being locked
- Deliver database (as SAS, SPSS, Text datasets)