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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
Full text: 1 Index: WPRIM Type of study: Guideline Language: Zh Journal: Acta Pharmaceutica Sinica Year: 2015 Type: Article