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12篇 您的检索式：作者名="DAVIT BM"

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		题名	作者	年代	出处	被引量
	1	Implementation of a reference-scaled average bioequivalence approach for highly vari- able generic drug products by the US Food and Drug Administra- tion显示文摘	DAVIT BM CHEN ML CONNER DP	2012	AAPS J2012，14，4：	1
	2	Highly variable drugs: observations from bioequivalence data submitted to the FDA for new generic drug applications 显示文摘	Davit BM Conner DP Fabian-Fritsch B	2008	AAPS J2008，10，1：	1
	3	Implementation of a reference-scaled average bioequivalence approach for highly variable generic drug products by the US Food and Drug Administration 显示文摘	Davit BM Chen ML Conner DP	2012	AAPS J2012，14，4：	1
	4	Bioequivalence approaches for highly variable drugs and drugproducts 显示文摘	Haidar SH Davit BM Chen ML	2008	Pharm Res2008，25，1：	1
	5	Implementation of a reference-scaled average bioequivalence approach for highly varia- ble generic drug products by the US Food and Drug Administra- tion显示文摘	DAVIT BM CHEN ML CONNER DP	2012	AAPS J2012，14，4：	1
	6	Comparing generic and innovator drugs: a review of 12 years of bioequivalence data from the United States Food and Drug Administration 显示文摘	Davit BM Nwakama PE Buehler GJ	2009	Center for Drug Evaluation and Research2009，43，10：	1
	7	Implementation of a reference-scaled average bioequivalence approach for highly vari- able generic drug products by the US Food and Drug Administra- tion显示文摘	DAVIT BM CHEN ML CONNER DP	2012	AAPS J2012，14，4：	1
	8	Survey of interna- tional regulatory bioequivalence recommendations for approval of generic topical dermatological drug products显示文摘	BRADDY AC DAVIT BM STIER EM	2015	AAPS J2015，17，1：	1
	9	Highly varia- ble drugs:observations from bioequivalence data submitted to the FDA for new generic drug applications 显示文摘	DAVIT BM CONNER DP FABIAN-FRITSCH B	2008	J2008，10，1：	1
	10	Highly variable drugs: observations from bioequivalence data submitted to the FDA for new generic drug applications 显示文摘	DAVIT BM CONNER DP FABIAN-FR1TSCH B	2008	AAPS J2008，10，1：	1
	11	Implementation of a reference-scaled average bioequivalence approach for highly var- iable generic drug products by the US Food and Drug Administra- tion显示文摘	DAVIT BM CHEN ML CONNER DP	2012	AAPS J2012，14，4：	1
	12	Implementation of a reference-scaled average bioequivalence approach for highly var- iable generic drug products by the US Food and Drug Administra- tion显示文摘	DAVIT BM CHEN ML CONNER DP	2012	AAPS J2012，14，4：	1

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