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検索結果 6 件

Guide to EU pharmaceutical regulatory law Seventh edition.

Guide to EU pharmaceutical regulatory law Seventh edition.
紙図書
editor, Sally Shorthose.Wolters Kluwer[2017]<AE5-541-B107>
国立国会図書館全国の図書館

Medical devices and the public's health : the FDA 510(k) clearance process at 35 years

Medical devices and the public's health : the FDA 510(k) clearance process at 35 years
紙図書
Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies.The National Academies Press[2011]<M361-B448>
国立国会図書館全国の図書館

Guide to EU pharmaceutical regulatory law Fourth edition.

Guide to EU pharmaceutical regulatory law Fourth edition.
紙図書
edited by Sally Shorthose.Wolters Kluwer Law & Business[2013]<AE5-541-B73>
国立国会図書館

Development and approval of combination products : a regulatory perspective / edited by Evan B. Siegel.

Development and approval of combination products : a regulatory perspective / edited by Evan B. Siegel.
紙図書
Wileyc2008.<SD81-B20>
国立国会図書館

Medical device regulations : global overview and guiding principles.

Medical device regulations : global overview and guiding principles.
紙図書
World Health Organizationc2003.<M361-B25>
国立国会図書館全国の図書館
  • 件名... -- standards. Device Approval -- legislation & jurisprudence. Device Approval -- standards....

Guide to EU pharmaceutical regulatory law / edited by Sally Shorthose.

Guide to EU pharmaceutical regulatory law / edited by Sally Shorthose.
紙図書
Kluwer Law Internationalc2010.<AE5-541-B53>
国立国会図書館全国の図書館

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