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- Health products policy and standards
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
- Health products policy and standards - World Health Organization (WHO)
The nomenclature of medical devices is a coding system used to generically identify medical devices and related health products
- Health products policy and standards - World Health Organization (WHO)
Regulation is primarily concerned with enabling patient access to high quality, safe and effective medical devices, and avoiding access to products that are unsafe When appropriately implemented, regulation ensures public health benefit and the safety of patients, health care workers and the community
- Substandard and falsified medical products - World Health Organization . . .
WHO fact sheet on substandard and falsified medical products, including key facts, scope of the problem, impacts, challenges and WHO response
- Regulating medical products - World Health Organization (WHO)
Regulating medical products Medicines WHO 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
- 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 the subject of medical products of this type The approved document on definitions is available at the following link: Working Definitions Document
- Regulation and Prequalification
Substandard and falsified medical products create many problems for both the individual taking the medicine and for families, the larger society, health care system and supply chain
- Medical Product Alert N°2 2024: Falsified OZEMPIC (semaglutide)
Alert SummaryThis WHO Medical Product Alert refers to three falsified batches of OZEMPIC (semaglutide) This falsified product has been detected in Brazil (October 2023), the United Kingdom of Great Britain and Northern Ireland (October 2023), and the United States of America (December 2023), and was supplied in the regulated supply chain OZEMPIC (semaglutide) is from a group of medicines
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