Medical devices - World Health Organization (WHO)
2024年6月16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
Substandard and falsified medical products - World Health …
2018年1月31日 · Substandard and falsified medical products may cause harm to patients and fail to treat the diseases for which they were intended. They lead to loss of confidence in medicines, healthcare providers and health systems. They affect every region of the world. Substandard and falsified medical products from all main therapeutic categories have been ...
Regulating medical products - World Health Organization (WHO)
2024年10月29日 · Medical devices. Regulation is primarily concerned with enabling patient access to high-quality, safe and effective medical devices, and restricting access to products that are unsafe or have limited clinical use. When appropriately implemented, regulation ensures public health benefit and the safety of patients, health care workers and the ...
Health products policy and standards - World Health Organization …
2011年4月6日 · Health products policy and standards. Our team provides authoritative guidance and standards on quality, safety and efficacy of health products and supports countries to formulate evidence-based policies and ensure good practice throughout the value chain. Assistive Technology. Medical devices. Essential Medicines.
Substandard and falsified medical products - World Health …
2024年6月20日 · Substandard and falsified medical products. Up to two billion people around the world lack access to necessary medicines, vaccines, medical devices including in vitro diagnostics, and other health products, which creates a vacuum that is too often filled by substandard and falsified products. This problem is growing as global supply chains ...
World Health Organization Medical products, vaccinations and …
Medical products, vaccinations and technologies. A well-functioning health system ensures equitable access to: essential medical products; vaccines; and. technologies of assured quality, safety, efficacy and cost-effectiveness, and their scientifically sound and cost-effective use.
1 in 10 medical products in developing countries is substandard or ...
2017年11月28日 · An estimated 1 in 10 medical products circulating in low- and middle-income countries is either substandard or falsified, according to new research from WHO. This means that people are taking medicines that fail to treat or prevent disease. Not only is this a waste of money for individuals and health systems that purchase these products, but ...
Health products policy and standards - World Health Organization …
The nomenclature of medical devices is a coding and naming system used to generically classify and identify all medical devices and related health products. According to different classification and nomenclature systems, there are between 5,000 to 24,000 different types of medical devices. They range from the very simple to complex, inexpensive ...
Medicines: Good manufacturing practices - World Health …
Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. The main risks are: unexpected contamination of products ...
Largest number of regulatory agencies for medical products …
2024年5月20日 · Español. WHO has approved designation of 33 national and regional regulatory authorities as WHO Listed Authorities (WLAs) that can be relied on for fulfilling the highest level of regulatory standards and practices for quality, safety and efficacy of medicines and vaccines. This listing makes a total of 36 regulatory authorities from 34 Member ...