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Displaying 51 - 60 of 119 results
Data recording by clinical trial staff
Procedure
A process for how clinical trial staff should record source and Case Record Form (CRF) data for trials
Version: 2.0
Author: WWARN
Malaria Case Record Form (CRF)
Procedure
Malaria Clinical Trial Case Record Form
Version: 2.0
Author: WWARN
Data management protocol generic
Procedure
Instruction to those data management team members delegated responsibility for producing and working on a data management protocol
Version: 2.0
Author: WWARN
Serious adverse event data reconciliation
Procedure
For when there is a need to reconcile safety data that are stored in two different databases during a clinical trial
Version: 2.0
Author: WWARN
Master validation plan
Procedure
For listing and documenting the objectives for all parties responsible for validation of computer equipment and software for a clinical trial
Version: v1.0
Author: WWARN
WWARN Malaria Data Dictionary
Procedure
Understand the data variables in data files
Version: 1.0
Author: Kalynn Kennon