Vertaling van "requirements on medicines " (Nederlands → Frans) :

The inspection units also support the Judicial Authority and are, in addition to their control and inspection tasks, responsible for dealing with and investigating any complaints relating to the legal requirements on medicines and/or health products.
The inspection units also support the Judicial Authority and are, in addition to their control and inspection tasks, responsible for dealing with and investigating any complaints relating to the legal requirements on medicines and/or health products.

In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.
In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.

The BUM department is legally required to provide support with putting online the list of medicines authorised in Belgium for new medicine MA and of the official information (Summary of Product Characteristics for healthcare professionals and leaflet for the general public).
The BUM department is legally required to provide support with putting online the list of medicines authorised in Belgium for new medicine MA and of the official information (Summary of Product Characteristics for healthcare professionals and leaflet for the general public).

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.

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).