DATA COLLECTION

WWARN

Standardised Malaria Clinical Trial CRF for the collection of relevant clinical data

• Questionnaires – GenMoz study (Appendix 5-8) 
• Case Report Form – MSMT study (Appendix 5)

WHO

Comprehensive set of globally applicable principles designed to guide stakeholders in the responsible collection, use, and sharing of human genome data.

Malaria GEN

Seeking consent for genomic research in developing countries – Template and Guidelines

Convention on Biological Diversity

Protocol on “Access to Genetic Resources and the Fair and Equitable Sharing of Benefits Arising from their Utilization to the Convention on Biological Diversity”. The Access and Benefit-sharing Clearing-House (ABSCH) is a platform facilitates the implementation of the Nagoya Protocol.

Global Alliance for Genomics & Health

Documents designed to help researchers and clinicians draft clear, informative consent forms

• Information sheets, inform consent and assent forms – GenMoz study (Appendx 1-4)
• Informed and assent forms – MSMT study (Appendix 3-4)