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Objectives and achievements of regulations in Japan

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References

  1. Worden A N and Roberts C N (1972). Experimental and Clinical Evaluations of Drugs and Drug Safety, Proceedings Japan — British Medical Symposium, Japan Medical Association, Tokyo 128–146

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  2. Takakura N (1987). Requirements for Pharmaceuticals and Medical Devices (Japan), Regulatory Affairs Professionals Society, November 19–20, San Francisco, USA

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  3. Shirota K (1986). Foreword, Pharmaceutical Administration in Japan, 3rd Edition, (Tokyo: Yakuji Nippo Ltd)

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  4. Roberts, C N (1980). GLP — The Management Viewpoint, Technical Seminar Text, British Medical Seminar, British Embassy, Tokyo

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  5. Roberts C N (1985a). Japan — regulations in the Land of the Rising Sun. BIRA J, 4 (1), 11–17

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  6. Roberts C N (1985b). International Aspects of GLP — the Japanese Situation, Proceedings of the Fourth International Meeting on Good Laboratory Practice, Cambridge, May 1985, pp. 53–72

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  7. Roberts C N (1986). Situations and predictions concerning Japan, Proceedings of 5th International Meeting on Good Laboratory Practice, Frankfurt, May 1986, pp. 176–198

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  8. Uchida K (1988). Acceptability of foreign clinical trial data in Japan. Drug Inf J, 22, 103–108

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© 1989 Kluwer Academic Publishers

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Roberts, C.N. (1989). Objectives and achievements of regulations in Japan. In: Walker, S.R., Griffin, J.P. (eds) International Medicines Regulations. CMR Workshop Series. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-0857-4_14

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  • DOI: https://doi.org/10.1007/978-94-009-0857-4_14

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-6873-4

  • Online ISBN: 978-94-009-0857-4

  • eBook Packages: Springer Book Archive

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