Vertaling van "registration marketing authorisation " (Nederlands → Frans) :

The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.
The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.

The Registration (marketing authorisation) department for its part is required to evaluate applications for a marketing authorisation (MA), for the sake of the National Procedure (NP), the European Decentralised Procedure (DCP), the Mutual Recognition Procedure (MRP) and the Central Procedure (CP).
The Registration (marketing authorisation) department for its part is required to evaluate applications for a marketing authorisation (MA), for the sake of the National Procedure (NP), the European Decentralised Procedure (DCP), the Mutual Recognition Procedure (MRP) and the Central Procedure (CP).

FIELDS OF COMPETENCY 19 Activities of the operational departments 20 R&D (research and development) 20 Registration (marketing authorisation) 22 Vigilance 28 Production & Distribution 30 Proper Use of Medicines 38
FIELDS OF COMPETENCY 19 Activities of the operational departments 20 R&D (research and development) 20 Registration (marketing authorisation) 22 Vigilance 28 Production & Distribution 30 Proper Use of Medicines 38

Transition and backlog In the first phase of the transition to a new structure for the FAMHP, the emphasis is on the reorganisation and restructuring of the Registration (marketing authorisation) department.
Transition and backlog In the first phase of the transition to a new structure for the FAMHP, the emphasis is on the reorganisation and restructuring of the Registration (marketing authorisation) department.

Simplified marketing authorisation (MA) for medicines for human use. Unique national registration number for medicines for human use.
Simplified marketing authorisation (MA) for medicines for human use. Unique national registration number for medicines for human use.

In 2007, 88 licences/registrations were issued to market participants For the export of precursors, 200 export authorisations and 11 import authorisations were issued.
In 2007, 88 licences/registrations were issued to market participants For the export of precursors, 200 export authorisations and 11 import authorisations were issued.