Medical devices - World Health Organization (WHO)
2021年6月30日 · WHA67.20 Regulatory system strengthening for medical products; WHA67.22 Access to essential medicines; WHA67.23 Health intervention and technology assessment in support of universal health coverage; WHA68.15 Strengthening emergency and essential surgical care and anaesthesia as a component of universal health coverage
Health products policy and standards - World Health Organization …
2011年4月6日 · Medical equipment is used for the specific purposes of diagnosis and treatment of disease or rehabilitation following disease or injury; it can be used either alone or in combination with any accessory, consumable or other piece of medical equipment. Medical equipment excludes implantable, disposable or single-use medical devices.
Substandard and falsified medical products - World Health …
2024年12月3日 · These products can be found in all countries, impacting all types of medical products, including life-saving treatments like vaccines, antibiotics and cancer therapies. In 2017, the World Health Organization estimated that 1 in 10 medicines in low- and middle-income countries failed quality control tests, suggesting the product is substandard ...
Regulating medical products - World Health Organization (WHO)
2024年10月29日 · 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 …
World Health Organization Medical products, vaccinations and …
Medical products, vaccinations and technologies. A well-functioning health system ensures equitable access to:
Definitions of Substandard and Falsified (SF) Medical Products
On 29 May 2017 at the Seventieth World Health Assembly, a decision was agreed to adopt “Substandard and Falsified (SF) medical products” as the term to be used in the name of the Member State mechanism and in all future documentation on …
Global Benchmarking Tools - World Health Organization (WHO)
The Global Benchmarking Tool (GBT) represents the primary means by which the World Health Organization (WHO) objectively evaluates regulatory systems, as mandated by WHA Resolution 67.20 on Regulatory System Strengthening for medical products. The tool and benchmarking methodology enables WHO and regulatory authorities to:
Substandard and falsified medical products: Scope, scale and harm
2019年12月9日 · Most commonly, SF medical products enter the legal supply chain at distribution level through hospitals, clinics, pharmacies and wholesalers, who have obtained medical products from unknown sources and intermediaries without checking their credentials or conducting any due diligence. Supply chains can be long and complex.
Health products policy and standards - World Health Organization …
WHA67.20 “Regulatory system strengthening for medical products” The 67th WHA approved the resolution “Regulatory system strengthening for medical products." It states the importance of regulations for medical devices as one of the medical products, for better public health outcome and to increase access to safe, effective and quality ...
Medicines: Good manufacturing practices - World Health …
2015年11月20日 · The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects.