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The Chilean Public Health Institute has released new informational material to guide implementation of regulations bringing medical devices and in vitro diagnostic medical devices under sanitary control.

On January 26th, 2016, Law N°20,894 was published in the Official Gazette. This law postpones enforcement of the mandate that would require independent employees to pay social security contributions.

Before a pesticide can be commercialized in Chile, it has to undergo a lab analysis first.

Chile's Public Health Institute has issued new requirements mandating pharmaceutical companies to submit digitized versions of their Professional Information Leaflets for publication on the ISP website. Marketing authorization holders must comply with specific formatting and submission procedures by December 31, 2026, or face potential administrative proceedings and sanctions.

Chile will open its borders to certain non-resident foreign nationals on Oct. 1, 2021. Individuals seeking to enter Chile on or after this date will have to meet the following compliance requirements:

Chile's Public Health Institute has opened a public consultation on updated guidance for its National Technovigilance System, establishing comprehensive post-market surveillance requirements for medical devices and in vitro diagnostics. The framework introduces stringent obligations for manufacturers, importers, and distributors, including mandatory technovigilance officer appointments, incident reporting timelines, and field safety corrective action protocols.

On December 11th, Decree No. 1 of the Ministry of Health (herein, the "Decree") was published on the Official Gazette.

On June 6th, 2015, Law No. 20,850, which creates the Financial Protection System for Diagnostics and Treatment of High Costs, and pays posthumous tribute to Luis Ricarte Soto Gallegos, has been published.

El Instituto de Salud Pública de Chile publicó material informativo para facilitar la implementación del Decreto Exento N°25/2026, que incorpora dispositivos médicos y de diagnóstico in vitro al régimen de control sanitario. El documento incluye una matriz organizativa por categorías, ejemplos de productos dentro y fuera del alcance normativo, y especificaciones sobre clases de riesgo y plazos de vigencia.

Medical devices are any instrument, apparatus, application, material or article, including software, used by themselves or in tandem, and defined by the manufacturer to be used directly on human beings.

El Instituto de Salud Pública de Chile ha establecido nuevos requisitos para los titulares de registros sanitarios de productos farmacéuticos, exigiendo el envío digitalizado de folletos de información profesional para su publicación en línea. ¿Cuáles son las obligaciones específicas, los plazos de cumplimiento y las consecuencias del incumplimiento de esta normativa sanitaria?

El Instituto de Salud Pública de Chile ha sometido a consulta pública una nueva Guía del Sistema Nacional de Tecnovigilancia que actualizará los estándares de vigilancia post-comercialización para dispositivos médicos. La guía establece obligaciones específicas para fabricantes, importadores y distribuidores, incluyendo la designación de responsables, sistemas de notificación y gestión de eventos adversos. ¿Cómo impactarán estos nuev

On March 29th, 2016, Ex.Ord 43 from the Ministry of Health was published in the Official Gazzette, which approves the Regulation for the Storage of Hazardous Substances.

On April 12, 2022, the Chilean government announced the implementation of a new framework to govern the country's border restrictions related to the COVID-19 pandemic.

With the development of Neuroscience in recent years, human beings can influence their own nervous system, especially the brain.

Con el desarrollo de la neurociencia en los últimos años, el ser humano puede influir sobre su propio sistema nervioso, especialmente sobre el cerebro.