検索ワード: elements (スペイン語 - オランダ語)

elements
punten

mida dels elements
formaat onderdelen

mira the elements en acción
bekijk the elements in actie

cofirmació per a suprimir múltiples elements
bevestig het wissen van meerdere onderdelen

limita la longitud de les pàgines a 100 elements
limiteer uitgebreide beschrijvingen tot 100 onderdelen

esteu segur que voleu suprimir aquests elements?
weet u zeker dat u de gekozen onderdelen wil wissen?

elevaciones - elementos vectoriales (elevation – vector elements)
hoogte – vectorelementen (elevation - vector elements)

benchmarks on rental values of particular network elements are irrelevant.
benchmarks on rental values of particular network elements are irrelevant.

under such circumstances, the notified measure can be assumed not to include state aid elements.
under such circumstances, the notified measure can be assumed not to include state aid elements.

cantidad de efecto de contraste inactivo@title: tab color transformations on disabled elements
sterkte van contrasteffect voor inactief@title:tab color transformations on disabled elements

moreover, liberalisation and network element unbundling have resulted in a variety of wholesale products which could serve as benchmarks for valuing the rental value of various infrastructure elements.
moreover, liberalisation and network element unbundling have resulted in a variety of wholesale products which could serve as benchmarks for valuing the rental value of various infrastructure elements.

se pondrán a disposición conjuntos de datos espaciales que describan la morfología de la batimetría utilizando al menos los tipos de objetos espaciales incluidos en el paquete elevation – grid coverage o en el paquete elevation – vector elements.
ruimtelijke gegevensverzamelingen die de morfologie van bathymetrie beschrijven moeten worden gegeven met ten minste het gebruik van de ruimtelijke objecttypes vervat in ofwel het pakket elevation – grid coverage of het pakket elevation – vector elements.

(6) among the criteria for the selection of the successful tenderers is the inclusion in the facility of elements of new technology or processes, whose trialling or demonstration will assist the development of sustainable processes in waste recycling.
(6) among the criteria for the selection of the successful tenderers is the inclusion in the facility of elements of new technology or processes, whose trialling or demonstration will assist the development of sustainable processes in waste recycling.

directrices definitivas • choice of control group in clinical trials (cpmp/ich/364/96), ich e10. • clinical investigation of medicinal products in children (cpmp/ich/2711/99), ich e11. • safety pharmacology studies for human pharmaceuticals (cpmp/ich/539/00), ich s7a. • stability testing guidelines: stability testing of new active substances and medicinal products (cpmp/ich/2736/99 rev. of cpmp/ich/380/95), ich q1ar. • non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals (cpmp/ich/286/95, modification), ich m3 modification. • reproductive toxicology: toxicity to male fertility (cpmp/ich/136/95 modification), ich s5b modification. • data elements for transmission of individual case safety reports (cpmp/ich/287/95 modification), ich e2b. • recommendations on electronic transmission of individual case safety reports message specification (cpmp/ich/285/95), ich m2. • good manufacturing practice guide for active pharmaceutical ingredients (cpmp/ich/4106/00), ich q7a. • common technical document (ctd) (cpmp/ich/2887/99), ich m4.
definitieve richtsnoeren ‘ choice of control group in clinical trials’ (cpmp/ ich/ 364/ 96), ich e10 ‘ clinical investigation of medical products in children’ (cpmp/ ich/ 2711/ 99), ich e11 ‘ safety pharmacology studies for human pharmaceuticals’ (cpmp/ ich/ 539/ 00), ich s7a ‘ stability testing guidelines: stability testing of new active substances and medicinal products’ (cpmp/ ich/ 2736/ 99 herziening van cpmp/ ich/ 380/ 95), ich q1ar ‘ non-clinical safety studies for the conduct of human clinical trials for pharmaceuticals’ (cpmp/ ich/ 286/ 95, wijziging), ich m3 wijziging ‘ reproductive toxicology: toxicity to male fertility’ (cpmp/ ich/ 136/ 95 wijziging), ich s5b wijziging ‘ data elements for transmission of individual case safety reports’ (cpmp/ ich/ 287/ 95 wijziging), ich e2b ‘ recommendations on electronic transmission of individual case safety reports message specification’ (cpmp/ ich/ 285/ 95), ich m2 ‘ good manufacturing practice guide for active pharmaceutical ingredients’ (cpmp/ ich/ 4106/ 00), ich q7a ‘ common technical document (ctd )’, (cpmp/ ich/ 2887/ 99), ich m4