Aplicación de inteligencia artificial para la Catedra Estructuras III . Facultad de Arquitectura y urbanismo. Universidad Nacional del Nordeste,

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

La campaña ha consistido en la revisión del etiquetado e instrucciones de uso de todos los ter- mómetros digitales comunicados, así como de la documentación técnica adicional de

You may wish to take a note of your Organisation ID, which, in addition to the organisation name, can be used to search for an organisation you will need to affiliate with when you

Where possible, the EU IG and more specifically the data fields and associated business rules present in Chapter 2 –Data elements for the electronic submission of information

The 'On-boarding of users to Substance, Product, Organisation and Referentials (SPOR) data services' document must be considered the reference guidance, as this document includes the

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

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