Looking for regulatory US requirements for medical gloves? Or how about the testing requirements within the EU? Find these answers and more in Industry Links – your go-to-resource for the most popular regulatory, government, industry, testing and health and safety websites.
REGULATORY
US Food and Drug Administration (FDA)
Regulates the sale and marketing of medical devices in the US.
Ministry of Health, Labour and Welfare (厚生労働省) - Japan
Provides regulations on maximum residue limits for agricultural chemicals in foods, basic food and drug regulations, standards for foods, food additives, etc.
Agência Nacional de Vigilância Sanitária (ANVISA) - Brazil
ANVISA is a regulatory body of the Brazilian government responsible for the regulation and approval of pharmaceutical drugs, sanitary standards and regulation of the food industry.
National Medical Products Administration (国家药品监督管理局) - China
The NMPA is responsible for registration of medical devices for the Chinese market. All medical devices have to be classified by the CFDA according to its risks.
The European Committee for Standardization or Comité Européen de Normalisation (CEN) provides an efficient infrastructure for the development of coherent sets of standards and specifications.
Establishes standards for medical gloves used by emergency medical personnel under NFP 1999: Standard on Protective Clothing for Emergency Medical Operations (US).