Guía para la aplicación de la norma ISO 22000:2005 a través de un diagnóstico de necesidades

If certification of devices under the MDR has not been finalised before expiry of the Directive’s certificate, and where the device does not present an unacceptable risk to health

Entre nosotros anda un escritor de cosas de filología, paisano de Costa, que no deja de tener ingenio y garbo; pero cuyas obras tienen de todo menos de ciencia, y aun

In medicinal products containing more than one manufactured item (e.g., contraceptive having different strengths and fixed dose combination as part of the same medicinal

Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in

Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in

This section provides guidance with examples on encoding medicinal product packaging information, together with the relationship between Pack Size, Package Item (container)

Package Item (Container) Type : Vial (100000073563) Quantity Operator: equal to (100000000049) Package Item (Container) Quantity : 1 Material : Glass type I (200000003204)

d) que haya «identidad de órgano» (con identidad de Sala y Sección); e) que haya alteridad, es decir, que las sentencias aportadas sean de persona distinta a la recurrente, e) que