Você procurou por: authorisation (Francês - Finlandês)

post-authorisation
ihmisille tarkoitettujen post- authorisation

marketing authorisation suspended
arketing arketing

marketing authorisation holder:
myyntiluvan haltija:

the marketing authorisation holder
35 myyntiluvan haltija alcon laboratories (uk) ltd.

marketing authorisation number(s)
myyntiluvan numero( t)

name of the marketing authorisation holder
myyntiluvan haltijan nimi

date of first authorisation: 10 mai 2010
myyntiluvan myöntämispäivä: 10 toukokuu 2010

date de première authorisation: 23/02/2012
ensimmäisen myyntiluvan myöntämispäivämäärä: 23/02/2012

name and address of the marketing authorisation holder
myyntiluvan haltijan nimi ja osoite

titulaire de l’ authorisation de mise sur le marché
myyntiluvan haltija

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

je ne peux pas vous laisser entrer sans authorisation adéquate!
teillä ei ole kulkulupaa.

marketing authorisation holder takeda pharma ges. m. b. h.
myyntiluvan haltija 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
european medicines agency

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
budjetti - ja tilinpitotiedot siirrettiin vuoden 1998 puolivälissä ja järjestelmä toimii nykyisin hyvin.

standard operating procedure on the release of assessment reports to applicants / marketing authorisation holders
note for guidance on plasma- derived medicinal products

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