Se2-2 How pharmaceutical companies meet the ICH guideline for reproductive toxicity studies. : Consideration from a survey carried out by JPMA(Proceedings of the 27th Annual Meeting)
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概要
- 論文の詳細を見る
- 日本トキシコロジー学会の論文
- 2000-10-31
著者
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Okuda Yasuyuki
Working Group For Reproductive Toxicology Non-clinical Evaluation Subcommitee Drug Evaluation Commit
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Hirano Fumiya
Drug Evaluation Committee The Japan Pharmaceutical Manufacturers Association (jpma):research & D
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Numa Toshiaki
Drug Evaluation Committee The Japan Pharmaceutical Manufacturers Association (jpma):toxicology Team
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Endo Y
Drug Evaluation Committee The Japan Pharmaceutical Manufacturers Association (jpma):clinical Safety
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Nishigaki K
Drug Evaluation Committee The Japan Pharmaceutical Manufacturers Association (jpma):fuji Research La
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MINESHIMA Hiroshi
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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NUMA Toshiaki
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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NISHIGAKI Keiji
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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ENDO Yoshihiko
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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OGASAWARA Hiroyuki
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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HIRANO Fumiya
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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MIYAKE Yukio
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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MATSUZAWA Toshiaki
Working Group for Reproductive Toxicology, Non-clinical Evaluation Subcommitee, Drug Evaluation Comm
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Matsuzawa T
Drug Evaluation Committee The Japan Pharmaceutical Manufacturers Association (jpma)
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Miyake Yukio
Working Group For Reproductive Toxicology Non-clinical Evaluation Subcommitee Drug Evaluation Commit
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Mineshima H
Drug Safety Res. Laboratories (kakamigahara) Eisai Co. Ltd.
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Ogasawara Hiroyuki
Drug Evaluation Committee The Japan Pharmaceutical Manufacturers Association (jpma):medical Research
関連論文
- A SURVEY OF THE VALUES OF CLINICAL CHEMISTRY PARAMETERS OBTAINED FOR A COMMON RAT BLOOD SAMPLE IN NINETY-EIGHT JAPANESE LABORATORIES
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- COLLABORATIVE WORK TO EVALUATE TOXICITY ON MALE REPRODUCTIVE ORGANS BY REPEATED DOSE STUDIES IN RATS : 21)COMPARISON OF THE EFFECTS OF 2-AND 4-WEEKS PYRIMETHAMINE TREATMENT IN RATS
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- REPRODUCTIVE TOXICITY MUTAGENICITY AND ANTIGENICITY OF PAMITFLPLASE (GENETICAL RECOMBINATION)
- Se2-2 How pharmaceutical companies meet the ICH guideline for reproductive toxicity studies. : Consideration from a survey carried out by JPMA(Proceedings of the 27th Annual Meeting)
- INTRAVENOUS SINGLE AND REPEATED DOSE TOXICITY STUDIES OF CIMADRONATE (YM175), A NOVEL BISPHOSPHONATE, IN RATS
- IMPACT OF GLOBALIZATION UNDER THE ICH GUIDELINES ON THE CONDUCT OF REPRODUCTIVE TOXICITY STUDIES : REPORT ON CURRENT STATUS IN JAPAN, EUROPE AND THE US BY QUESTIONNAIRE SURVEY
- P-82 Collaborative work to evaluate toxicity on male reproductive organs by repeated dose studies in rats. : Fadrozole hydrochloride : An oral 2/4-week male reproductive organ toxicity study(Proceedings of the 27th Annual Meeting)
- COLLABORATIVE WORK TO EVALUATE TOXICITY ON MALE REPRODUCTIVE ORGANS BY REPEATED DOSE STUDIES IN RATS : 4)FADROZOLE HYDROCHLORIDE : AN ORAL 2/4-WEEK MALE REPRODUCTIVE ORGAN TOXICITY STUDY
- INTRAVENOUS SINGLE AND REPEATED DOSE TOXICITY STUDIES OF CIMADRONATE (YM175), A NOVEL BISPHOSPHONATE, IN RATS