Procedures

WWARN is continually updating a library of standardised procedures that offer guidance in the execution of various activities in the fields of clinical, in vitro, pharmacology, data collection and molecular analysis for antimalarial drug resistance researchers. Please read our tools and resources usage guidance.

For resources that relate to other infectious and emerging diseases, visit iddo.org.

Publication Code: DMSTAT01

Instruction to those data management team members delegated responsibility for producing and working on a data management protocol

Version: 2.0

Author(s): WWARN

Publication Code: AD07

A process for ensuring that issues such as stock, equipment, staff, participants and venue are adequately prepared for scheduled ward admission periods

Version: 2.0

Author(s): WWARN

Publication Code: AD04

A process for ensuring that stock, equipment, documentation, staff and venue are adequately prepared for a new clinical trial

Version: 2.0

Author(s): WWARN

Malaria Clinical Trial Case Record Form

Version: 2.0

Author(s): WWARN

Publication Code: PHA_DM03

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(s): WWARN

Understand the data variables in data files

Version: 1.0

Author(s): Kalynn Kennon

Publication Code: DMSTAT03

Receiving, data entry and validating data within a clinical trial

Version: 2.0

Author(s): WWARN

Publication Code: AD01

Some basic guidelines for team members responsible for project management

Version: 2.0

Author(s): WWARN

Publication Code: QA01

A system for applying quality management at the trial site so there is effective compliance with sponsor, applicable regulatory and ethical requirements

Version: 2.0

Author(s): WWARN

Publication Code: QA06

For when an investigator/institution takes responsibility for setting up and maintaining the sponsor file

Version: 2.0

Author(s): WWARN