PUNTO 3 INFORME DE LOS CONSEJEROS UNIVERSITARIOS

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

In addition to the requirements set out in Chapter VII MDR, also other MDR requirements should apply to ‘legacy devices’, provided that those requirements

The notified body that issued the AIMDD or MDD certificate may confirm in writing (after having reviewed manufacturer’s description of the (proposed) change) that the

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

Las manifestaciones musicales y su organización institucional a lo largo de los siglos XVI al XVIII son aspectos poco conocidos de la cultura alicantina. Analizar el alcance y

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

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)