Why GLP
Regulatory-grade product evaluation.
OECD Good Laboratory Practice (GLP) is a regulatory quality system required for studies that support the World Health Organization (WHO) prequalification of vector control products, including insecticide-treated nets (ITNs), indoor residual spraying (IRS) products, spatial repellents, and other vector control tools.
Why GLP
GLP ensures that:
- Studies are planned, conducted, monitored, recorded, reported, and archived in a standardised and transparent manner
- Data integrity, traceability, and reproducibility are assured
- Study results are acceptable to WHO review bodies, national regulatory authorities, and international procurement agencies
By conducting studies under GLP, AIRID enables partners to generate regulatory-grade evidence suitable for WHO prequalification, regulatory review, and policy decision-making.