All documents were published by the Costa Rican Ministry of Health and are in PDF format. The Costa Rica Ministry of Health updates their database of approved devices on a monthly basis: Costa Rica Ministry of Health database of approved dev
Swissmedic is the regulatory agency responsible for authorizing and supervising therapeutic products in Switzerland.
In Malaysia, general medical and IVD devices are regulated by the Medical Device Authority (MDA) of the Ministry of Health. The regulatory framework is based on the Medical Device Act 2012 (Act 737) and Medical Device Regulations 2012 and closely follows GHTF guidelines. The legislation came into effect on July 1, 2013.
The Health and Youth Care Inspectorate (Inspectie Gezondheidszorg en Jeugd or IGJ) is the Dutch government agen
The Department of Planning and Organization of the National Health Service (Il Dipartimento della programm
The Spanish Agency for Medicine and Health Products (Agencia Española de Medicamentos y Productos Sanitarios or AEMPS) is the regulatory agency that overs
The Medicines and Healthcare Products Regulatory Agency (MHRA) is the government agency that regulates pharmaceuticals, blood establishments, advanced th