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EudraLex is the collection of rules and regulations governing medicinal products in the European Union. ==Volumes== EudraLex consists of 10 volumes: *Concerning Medicinal Products for Human use: * *Volume 1 - Pharmaceutical Legislation. * *Volume 2 - Notice to Applicants. * * *Volume 2A deals with procedures for marketing authorisation. * * *Volume 2B deals with the presentation and content of the application dossier. * * *Volume 2C deals with Guidelines. * *Volume 3 - Guidelines. *Concerning Medicinal Products for human use in clinical trials (investigational medicinal products). * *Volume 10 - Clinical trials. *Concerning Veterinary Medicinal Products: * *Volume 5 - Pharmaceutical Legislation. * *Volume 6 - Notice to Applicants. * *Volume 7 - Guidelines. * *Volume 8 - Maximum residue limits. 抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「EudraLex」の詳細全文を読む スポンサード リンク
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