전문 번역가, 번역 회사, 웹 페이지 및 자유롭게 사용할 수 있는 번역 저장소 등을 활용합니다.
irlande: clinical pharmacology and therapeutics
irland: clinical pharmacology and therapeutics
마지막 업데이트: 2014-10-23
사용 빈도: 1
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royaume-uni: clinical pharmacology and therapeutics
vereinigtes königreich: clinical pharmacology and therapeutics
마지막 업데이트: 2014-10-23
사용 빈도: 1
품질:
1 coetzee et al, 2007, journal of veterinary pharmacology & therapeutics, 30, 4, 305-319.
1 coetzee et al., 2007, journal of veterinary pharmacology & therapeutics, 30, 4, 305-319.
마지막 업데이트: 2011-10-23
사용 빈도: 1
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lignes directrices finales — 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
endgültige leitlinien • 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. von 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
마지막 업데이트: 2011-10-23
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