International Comparative Legal Guide to Drug & Medical Device Litigation 2020: Chapter 3 Argentina
por Ana Andrés
INTERNATIONAL COMPARATIVE LEGAL GUIDELINES
The main regulatory body that applies to the regulation of pharmaceutical products, medical devices, supplements, over-the-counter products and cosmetics is the Ministry of Health. Nevertheless, due to the fact that said Ministry also covers many areas, such as all matters related to health regulations, a specific administrative body has been created to deal with matters related to the registration, maintenance and all other aspects concerning pharmaceutical products, medical devices, supplements, over-the-counter products and cosmetics. This Administrative Body is the National Administration of Medicines, Food and Medical Technology (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica), commonly referred to as ANMAT…
Publicado y reproducido con el permiso de Global Legal Group Ltd, Londres. Este artículo fue publicado primero en ICLG to: Drug & Medical Device Litigation 1ª Edición.
Palabras clave: Derecho de la Salud · Life Sciences
International Comparative Legal Guide to Drug & Medical Device Litigation 2020: Chapter 3 Argentina
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