Você procurou por: therapeutic (Húngaro - Inglês)

therapeutic goods act 1989
therapeutic goods act 1989,

therapeutic goods (charges) act 1989
therapeutic goods (charges) act 1989,

therapeutic goods and cosmetics act, 1986
therapeutic goods and cosmetics act, 1986,

therapeutic goods (manufacturing principles) determinations
therapeutic goods (manufacturing principles) determinations,

therapeutic products programme, health canada, ottawa
therapeutic products programme, health canada, ottawa

therapeutic goods (excluded goods) order no.
therapeutic goods (excluded goods) order no 1 of 1992,

australian code of good manufacturing practice for therapeutic goods – medicinal gases, july 1992
australian code of good manufacturing practice for therapeutic goods - medicinal gases, july 1992

australian code of good manufacturing practice for therapeutic goods – sunscreen products, february 1994
australian code of good manufacturing practice for therapeutic goods - sunscreen products, february 1994

(1946) "curare a review of its therapeutic effects and their physiological basis.
(1946) "curare a review of its therapeutic effects and their physiological basis.

1 of 1992 - therapeutic goods (goods that are not therapeutic devices) order no. 1 of 1992
therapeutic goods (goods that are not therapeutic devices) order no 1 of 1992,

ausztráliában a gyártási minőség ellenőrzéséért felelős személyeket a therapeutic goods act 1989 szerint a therapeutic goods regulation 19. cikkének b) bekezdése határozza meg.
in australia, the responsible persons are for manufacturing quality control as specified in the therapeutic goods regulation 19(b) under the therapeutic goods act 1989.

ha egy orvostechnikai eszköz olyan kiegészítő gyógyhatású anyagot tartalmaz, amely szerepel az európai gyógyszerkönyv leírásaiban, a therapeutic goods administration konzultál az európai közösség gyógyászati termékek forgalomba hozatalának engedélyezéséért felelős illetékes hatóságával.
if a medical device incorporates a substance with ancillary medicinal action other than one specified in the european pharmacopoeia, the therapeutic goods administration shall carry out such consultation with one of the competent authorities within the european community responsible for authorising the placing on the market of medicinal products.

a felek elismerik, hogy a termékek piaci felügyelet céljából történő regisztrációja vagy jegyzékbe vételére vonatkozó, a therapeutic goods act szerinti ausztrál, valamint a megfelelő európai közösségi eljárásokat e megállapodás nem érinti.
the parties recognise that australian procedures under the therapeutic goods act for the registration or listing of products for market surveillance purposes, and corresponding european community procedures, are unaffected by this agreement.

a csoport a health canada gyógyászati termékek programja (therapeutic products programme), az európai közösség és a megfelelő ek-hatóságok képviselőit foglalja magába.
the group will include representatives of the therapeutic products programme in health canada, of the european commission, and of the relevant ec authorities.

director-general, therapeutic products programme, health canada, 2nd floor, health protection building, al: 0702a, tunney's pasture, ottawa, ontario, k1a ol2, canada.
the director-general, therapeutic products programme, health canada, 2nd floor, health protection building, al: 0702a, tunney's pasture, ottawa, ontario, k1a ol2, canada.