Good manufacturing practices : medicinal products for human and veterinary use

書誌事項

Good manufacturing practices : medicinal products for human and veterinary use

European Commission, Directorate General III - Industry Pharmaceuticals and Cosmetics

(The Rules governing medicinal products in the European Union, v. 4)

Office for Official Publications of the European Communities, 1998

1997 ed

タイトル別名

Eudralex

Pharmaceutical legislation

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内容説明・目次

内容説明

This guide to medicinal products features chapters headed by a principle of GMP, outlining the Quality Assurance objectives of that chapter and a text which aims to provide sufficient detail for manufacturers to be made aware of essential matters to be considered when implementing the principle.

目次

  • Directives. Good manufacturing practices. Basic requirements: quality management
  • personnnel
  • premises and equipment
  • documentation
  • production
  • quality control
  • contract manufacture and analysis
  • complaints and product recall
  • self inspection.

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詳細情報

  • NII書誌ID(NCID)
    BA35115352
  • ISBN
    • 9282820297
  • 出版国コード
    lu
  • タイトル言語コード
    eng
  • 本文言語コード
    eng
  • 出版地
    Luxembourg
  • ページ数/冊数
    x, 143 p.
  • 大きさ
    30 cm
  • 親書誌ID
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