Vertaling van "manufacturers of medicines " (Nederlands → Frans) :

TERMINOLOGIE

tandheelkundig 'chairside'-systeem voor CAD (computer-aided design) en CAM (computer-aided manufacturing)
fauteuil de système de CAO/FAO dentaire

tandheelkundig systeem voor CAD (computer-aided design) en CAM (computer-aided manufacturing) vervaardigd in laboratorium
laboratoire de système de CAO/FAO dentaire

applicatiesoftware voor tandheelkundig CAD/CAM (computer-aided design / computer-aided manufacturing)-systeem
logiciel de CAO/FAO

IN-CONTEXT TRANSLATIONS

The external services of Unit II inspect manufacturers of medicines (in Belgium and non-EU countries), the wholesalers, the recognised laboratories, the companies recognised on the basis of the royal decree on raw materials used by the pharmacist, the manufacturers of “Active Pharmaceutical Ingredient” (API), blood establishments and cell and tissue banks.
The external services of Unit II inspect manufacturers of medicines (in Belgium and non-EU countries), the wholesalers, the recognised laboratories, the companies recognised on the basis of the royal decree on raw materials used by the pharmacist, the manufacturers of “Active Pharmaceutical Ingredient” (API), blood establishments and cell and tissue banks.

If a non-conforming medicine is marketed outside Belgium and the medicine manufacturer is based in Belgium, the FAMHP is responsible for alerting other medicine authorities via the RAS.
If a non-conforming medicine is marketed outside Belgium and the medicine manufacturer is based in Belgium, the FAMHP is responsible for alerting other medicine authorities via the RAS.

Unit II Unit II is responsible for: ●● The recognition of industrial pharmacists ●● The granting of authorisations for the manufacture, import, export, wholesale, distribution of medicines ●● Dealing with quality problems (RAS – Rapid
Unit II Unit II is responsible for: ●● The recognition of industrial pharmacists ●● The granting of authorisations for the manufacture, import, export, wholesale, distribution of medicines ●● Dealing with quality problems (RAS – Rapid

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.

–– Het European Directorate for the Quality of Medicines (EDQM), groep Homeopathic Manufacturing Methods (HMM), voor de algemene monografie met betrekking tot de bereidingsmethodes van homeopathische stamproducten en de deconcentratie;
–– L’European Directorate for the Quality of Medicines (EDQM), groupe Homeopathic Manufacturing Methods (HMM), pour la monographie générale relative aux méthodes de préparation de souches homéopathiques et déconcentration ;