Hai cercato la traduzione di authorisation da Francese a Greco

post-authorisation
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marketing authorisation holder:
Κάτοχος άδειας κυκλοφορίας:

the marketing authorisation holder
36 Κάτοχος αδείας κυκλοφορίας

marketing authorisation number(s)
ΑΙ ΡΘΜΟΣ ΙΑ Ε Α Κ ΚΛ

the marketing authorisation holder fabricant
Κάτοχος αδείας κυκλοφορίας Παραγωγός

date de première authorisation: 23/02/2012
Ημερομηνία 1ης έγκρισης: 23/02/2012

name and address of the marketing authorisation holder
Ι Ι Υ Ν Η ΟΥ Τ Ο ΗΣ Δ Ι Σ Κ ΟΦΟΡΑ ΙΣ

titulaire de l’ authorisation de mise sur le marché
Κάτοχος της Άδειας Κυκλοφορίας

notice to marketing authorisation holders – pharmacovigilance guidlines
notice to marketing authorisation holders – pharmacovigilance guidlines

marketing authorisation holder takeda pharma ges. m. b. h.
takeda pharma ges. m. b. h.

european medicines agency post-authorisation evaluation of medicines for human use
european medicines agency post- authorisation evaluation of medicines for human use

the european medicines agency pre-authorisation evaluation of medicines for human use
the european medicines agency pre- authorisation evaluation of medicines for human use

excipients in the dossier for application for marketing authorisation for veterinary medicinal products.
excipients in the dossier for application for marketing authorisation for veterinary medicinal products.

note for guidance on stability testing for a adoptée en avril 1998 type ii variation to a marketing authorisation
note for guidance on stability testing for a type ii variation to a marketing authorisation

standard operating procedure on the release of assessment reports to applicants / marketing authorisation holders
standard operating procedure on the release of assessment reports to applicants / marketing au thorisation holders

the european agency for the evaluation of medicinal products pre-authorisation evaluation of medicines for human use
the european agency for the evaluation of medicinal products pre- authorisation evaluation of medicines for human use

pre-authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products
pre- authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products

carcinogenicity testing pre-authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products
carcinogenicity testing pre- authorisation studies to assess the potential for resistance resulting from the use of antimicrobial veterinary medicinal products Κοινή οµάδα εργασίας cpmp/ cvmp για την ποιότητα

notice to marketing authorisation holders (for inclusion in volume 9 of the rules governing medicinal products for human use)
Κατευθυντήριες γραµµές notice to marketing authorisation holders (for inclusion in volume 9 of the rules governing medicinal products for human use)

position paper on the regulatory requirements for the authorisation of low-dose modified release asa formulations in the secondary prevention of cardiovascular events.
position paper on the regulatory requirements for the authorisation of low- dose modified release asa formulations in the secondary prevention of cardiovascular events.