Key factors in design of case report form / 药学学报
Acta Pharmaceutica Sinica
; (12): 1452-5, 2015.
Article
in Zh
| WPRIM
| ID: wpr-505005
Responsible library:
WPRO
ABSTRACT
Case report form (CRF) is a key document for data collection in clinical trials. A well-designed CRF is required for database construction, data accuracy, data query/cleaning, CRF completion and statistical analysis. A well-defined process or SOP should be in place for CRF design. Data collection should fully meet the demand of study protocol. The layout of CRF should be clear with well-structured fields and standard coding for fields.
Full text:
1
Index:
WPRIM
Type of study:
Guideline
Language:
Zh
Journal:
Acta Pharmaceutica Sinica
Year:
2015
Type:
Article