Pharmaceutical products: Classified under Chapter 30 of the Harmonized System or Customs Tariff

Proyecto de Reglamento para el registro, control y vigilancia sanitaria de los dispositivos médicos de diagnóstico in vitro (Draft Regulations on the registration, control and sanitary surveillance of in vitro diagnostic medical devices) (89 pages, in Spanish)

The purpose of the notified draft Regulations is to establish the regulatory provisions for Law No. 29459 - Law on pharmaceutical products, medical devices and sanitary products - governing the registration, control and sanitary surveillance of in vitro diagnostic medical devices, and accessories thereof, to ensure their safety and performance, with a view to protecting public health.