医薬品の後期開発段階...

医薬品の後期開発段階における生物学的同等性評価に関するガイドラインの必要性及び溶出試験の役割について

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医薬品の後期開発段階における生物学的同等性評価に関するガイドラインの必要性及び溶出試験の役割について

Call No. (NDL)
Z19-834
Bibliographic ID of National Diet Library
11077761
Material type
記事
Author
嶋澤 るみ子
Publisher
東京 : 日本公定書協会
Publication date
2011
Material Format
Paper
Journal name
医薬品医療機器レギュラトリーサイエンス = Pharmaceutical and medical device regulatory science 42(4) 2011
Publication Page
p.300~304
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Paper

Material Type
記事
Author/Editor
嶋澤 るみ子
Author Heading
Alternative Title
Bioequivalence studies in late development phase: the necessity of guidelines and the role of dissolution test
Periodical title
医薬品医療機器レギュラトリーサイエンス = Pharmaceutical and medical device regulatory science
No. or year of volume/issue
42(4) 2011
Volume
42
Issue
4
Pages
300~304