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The who collaborative registration procedure (crp) is a reliance and collaboration mechanism to facilitate and accelerate the assessment and registration of medical products in participating countries Effective regulatory systems are an essential component of health systems and contribute to desired public health outcomes and innovation. Through crp, national regulatory authorities (nras) can access product assessment reports from stringent regulatory authorities (sras) or who prequalification, allowing for a faster.
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Regulation and prequalification progress towards enhancing regulatory practices related to medical products around the world is supported by capacity building, promoting regulatory convergence and harmonization. Who global benchmarking tools (gbt) for evaluation of national regulatory systems regulatory systems play a key role in assuring the quality, safety, and efficacy of medical products Its objective is to work with member states in improving the quantity, quality and analysis of accurate data concerning sf medical products, and to use that data in the better prevention, detection and response to those products, in order to protect public health.
Medical products may be subjected to various risks at different stages in the supply chain, for example, purchasing, storage, repackaging, relabelling, transportation and distribution.
Medicineswho plays a vital role in the regulation of medical products At the global level, who works to develop internationally recognized norms, standards and guidelines for medicine quality, safety and efficacy At the country level, who provides guidance, technical assistance and training to enable countries to implement these guidelines in the context of their own specific regulatory. About us assistive technology medical devices essential medicines
Who fact sheet on substandard and falsified medical products, including key facts, scope of the problem, impacts, challenges and who response.
