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Este documento de la Agencia Española de Medicamentos y Productos Sanitarios (AEMPS) es una traducción no oficial del publicado por la Comisión Europea (CE), que recoge las preguntas y respuestas que pueden ser formuladas con más frecuencia, en relación con la implementación de las normas relativas a los dispositivos de seguridad de medicamentos de uso humano.
Etiquetas: 27 de febrero 2018, Agencia, de seguridad, dispositivos, Documento, Madrid, medicamentos, Productos, Sanidad, Sanitarios, Uso humano.
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