Resources

This tool is a national-level quantification tool for basic neonatal resuscitation commodities, although it can be helpful for the district and facility level. It is designed only to provide estimates of product quantities for planning and cost simulations and is not intended for planning detailed distribution. The format of the tool includes simple design elements, such as graphics and navigation arrows, to guide users through the tool.

This guide provides an overview of water-filter products within PATH's Springboard Initiative ecosystem that feature the PATH-developed C1 Common Interface—a common-connection point and platform solution to promote product interchangeability, standardization, and market efficiency. Cartridges from one manufacturer can be used in water filters from another. This guide is primarily intended for professionals who seek balanced, introductory-level information on available water-filter products appropriate for low- and/or lower-middle income consumers in developing countries. It is not comprehensive and covers only products with the C1 Common Interface. The information presented is appropriate for commercial, public-sector, or nonprofit organizations interested in wholesale quantities.

This fact sheet describes a new ecosystem of interchangeable water-filter products from a range of companies based on the PATH-developed C1 Common Interface—a simple, common-connection point and platform solution designed to work with different filters and different devices.

PATH and Novo Nordisk are collaborating on the No Empty Shelves: Diabetes Supplies, There When Needed project. This case study describes our corporate partnership, which aims to raise awareness of noncommunicable diseases and improve understanding of the barriers that limit access to drugs and technologies for diabetes in low-resource settings.

The regulation of health technologies is a critical component of every country’s public health system and ensures that high-quality, safe health technologies reach the people who need them most. To harness momentum for regulatory harmonization, the Pan-African Parliament, New Partnership for African Development, and African Union Commission spearheaded the development of the African Union Model Law on Medical Products Regulation, which guides member states and regional economic communities in harmonizing regulatory systems and providing an enabling environment for the development and scale-up of health technologies.