Multimedia educativa para el estudio de los contenidos de la asignatura Odontopediatra

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)

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

 Tejidos de origen humano o sus derivados que sean inviables o hayan sido transformados en inviables con una función accesoria..  Células de origen humano o sus derivados que

En este sentido, puede defenderse que, si la Administración está habilitada normativamente para actuar en una determinada materia mediante actuaciones formales, ejerciendo

Este mismo régimen de deberes tiene sentido cuando la actuación de reforma o renovación significa un cambio radical de la morfología urbana, normalmente acompa- ñado por un cambio