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The South African Health Products Regulatory Authority (SAHPRA) is the organisation in charge of regulating the use of all Health Products throughout the country. It is part of the National Department of Health .
The National Forensic DNA Database of South Africa (NFDD) is a national DNA database used in law enforcement in South Africa.The Criminal Law (Forensic Procedures) Amendment Act No. 37 of 2013 (the "DNA Act") provides for the expansion and administration of such a database in South Africa, enabling the South African Police Service (SAPS) to match forensic DNA profiles derived from samples ...
National Drug Code (NDC) — administered by Food and Drug Administration. [1] Drug Identification Number (DIN) — administered by Health Canada under the Food and Drugs Act; Hong Kong Drug Registration — administered by the Pharmaceutical Service of the Department of Health (Hong Kong) National Pharmaceutical Product Index - South Africa
It was created by merging the South African Institute for Medical Research (SAIMR), the National Centre for Occupational Health and the National Institute for Virology. It also absorbed various provincial health department and university-run pathology laboratories. [4] The NHLS is the diagnostic pathology service for the public sector in South ...
The National Institute for Communicable Diseases (NICD) is the national public health institute of South Africa, [1] providing reference to microbiology, virology, epidemiology, surveillance and public health research to support the government's response to communicable disease threats. [2] [3]
South Africa's Medicines and Related Substance 1997 is a law enacted a compulsory license in order to fight HIV/AIDS epidemic. The intent of the Act was to reduce drug prices by allowing generic substitution of off-patent drugs, the parallel importation of on-patent drugs as well as price transparency.
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The registry traces back to the Health Omnibus Programs Extension Act of 1988 (HOPE or Public Law 100-607) which mandated the development of a database of AIDS Clinical Trials Information System. It would later be expanded under the Food and Drug Administration Modernization Act of 1997 (FDAMA or Public Act 105-115).