Traduction de «follows the guidelines authorised » (Néerlandais → Français) :

Mdeon follows the guidelines authorised in connection with its recognition and ensures strict compliance with the legal requirements (article 10 of the law of 25 March 1964 on medicines).
Mdeon follows the guidelines authorised in connection with its recognition and ensures strict compliance with the legal requirements (article 10 of the law of 25 March 1964 on medicines).

The Production & Distribution department of the FAMHP is responsible firstly for overseeing the conformity to current standards, guidelines and legal requirements for the manufacture, distribution and dispensing of medicines and health products and secondly for granting authorisations, recognitions and certificates, as well as for combating illegal practices and monitoring pharmacies.
The Production & Distribution department of the FAMHP is responsible firstly for overseeing the conformity to current standards, guidelines and legal requirements for the manufacture, distribution and dispensing of medicines and health products and secondly for granting authorisations, recognitions and certificates, as well as for combating illegal practices and monitoring pharmacies.

This calls for a guideline on optimal care that groups together the necessary indicators to assess the follow-up of the quality of care, as well as an inventory of the different persons involved and their specific skills, a distribution of the tasks, including a communication strategy and a co-ordination task, a precise list of the health professionals and other organisations involved, and adequate means to support the completion of these tasks.
Ceci requiert une directive de soins optimaux, reprenant des indicateurs nécessaires pour évaluer le suivi de la qualité des soins, un inventaire des différentes personnes impliquées et leurs compétences spécifiques, une répartition des tâches, y compris une stratégie de communication et une mission de coordination, une liste précise des professionnels de la santé et des organisations concernés, et les moyens adéquats pour soutenir la finalisation des tâches.

The application was withdrawn following the Committee for Medicinal Products for Human Use (CHMP) request to provide additional data satisfying the relevant EU guidelines.
Cette décision est survenue à la suite de la demande du CHMP (Comité européen pour les produits médicaux à usage humain) de fournir des données supplémentaires afin de satisfaire aux directives de l'UE.