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.
Pages
Extraction and storage of genetic material
A general process for collecting and processing of genetic material from blood samples in clinical trials
Version: 2.0
Author: WWARN Blood PK sample processing and transport
A process for taking pharmacokinetic samples from the participant through an interim processing laboratory and onto an analytical laboratory
Version: 2.0
Author: WWARN Clinical conduct of scheduled admission periods
A process for ensuring that scheduled ward admission periods are conducted appropriately
Version: 2.0
Author: WWARN Follow-up visits
A process for preparing for and conducting participant follow-up visits during a clinical trial
Version: 2.0
Author: WWARN Informed consent
A suggested process for how informed consent may be obtained from competent adults in a typical antimalarial clinical trial
Version: 2.0
Author: WWARN Screening visits
A process for preparing for and conducting participant screening during a clinical trial
Version: 2.0
Author: WWARN Clinical trial project management
Some basic guidelines for team members responsible for project management
Version: 2.0
Author: WWARN Identifying critical suppliers of trial services
A process for sites to use when identifying and managing critical service providers/vendors
Version: 2.0
Author: WWARN Trial staff training
A process for how training of trial staff will be planned and documented
Version: 2.0
Author: WWARN Data recording by clinical trial staff
A process for how clinical trial staff should record source and Case Record Form (CRF) data for trials
Version: 2.0
Author: WWARN Pages
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