Programa de capacitación para la mejora del clima organizacional con perspectiva de género para el personal docente y administrativo de la FCA

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

E Clamades andaua sienpre sobre el caua- 11o de madera, y en poco tienpo fue tan lexos, que el no sabia en donde estaña; pero el tomo muy gran esfuergo en si, y pensó yendo assi

diabetes, chronic respiratory disease and cancer) targeted in the Global Action Plan on NCDs as well as other noncommunicable conditions of particular concern in the European

 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

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)