Zambia’s ZAMRA and NHRA sign agreement on clinical trial oversight
Zambia’s Medicines Regulatory Authority (ZAMRA) and National Health Research Authority (NHRA) have signed a memorandum of understanding on the authorisation
Zambia’s Medicines Regulatory Authority (ZAMRA) and National Health Research Authority (NHRA) have signed a memorandum of understanding on the authorisation
Botswana’s medicines regulator has told importers, clearing agents and port of entry authorities that nine categories of medical devices and
South Africa’s Health Products Regulatory Authority (SAHPRA) has retained WHO Maturity Level 3 (ML3) for the regulation of vaccines as
Botswana’s medicines regulator has opened draft regulations under the Medicines and Related Substances Act 2025 for stakeholder comment, setting the
The Pharmacy and Poisons Board says the projects, ranging from a penicillin plant to vaccine and KEMRI facilities, support a target of producing half of essential health products locally.
MUMBAI, India — The Maharashtra Food and Drug Administration (FDA) has cancelled the drug sale licences of a Carrying and Forwarding
The authority becomes the tenth in Africa and the first in a Portuguese-speaking African country to reach ML3, covering medicines and imported vaccines.
EFDA assessed its system for devices and in vitro diagnostics against more than 250 WHO indicators, setting a roadmap towards formal benchmarking after reaching Maturity Level 3 for medicines last year.
The regulator has also issued the country’s first Good Pharmacy Practice standards and says it is supporting 13 new manufacturers, as it sets out its record at the Kenya Health Summit.
The agency put the value of the consignment at 301.1 billion naira and carried out the destruction under a Federal High Court order, with opioids among the substances.