Vertaling van "within the registration department " (Nederlands → Frans) :

Other concrete initiatives were also taken to increase the effectiveness of the FAMHP, such as the stabilisation and improvement of the MeSeA system, as well as the commencement of a new project to clear the backlogs within the Registration department within the entity for medicines for human use.
Other concrete initiatives were also taken to increase the effectiveness of the FAMHP, such as the stabilisation and improvement of the MeSeA system, as well as the commencement of a new project to clear the backlogs within the Registration department within the entity for medicines for human use.

The increased productivity is the result of concrete measures within the Registration department and has ensured that more MA are issued for medicines.
The increased productivity is the result of concrete measures within the Registration department and has ensured that more MA are issued for medicines.

As far as possible, similar activities will be grouped together within the same department.
As far as possible, similar activities will be grouped together within the same department.

Efficient cooperation between the departments within a pillar and with relevant departments in the other pillars must be ensured.
Efficient cooperation between the departments within a pillar and with relevant departments in the other pillars must be ensured.

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

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).