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000720623 020__ $$z9783954891870
000720623 020__ $$z9783954896875 (PDF)
000720623 035__ $$a(CaPaEBR)ebr10856569
000720623 035__ $$a(OCoLC)878147377
000720623 040__ $$aCaPaEBR$$beng$$erda$$epn$$cCaPaEBR
000720623 05014 $$aRS189$$b.O863 2014eb
000720623 08204 $$a572$$223
000720623 1001_ $$aOsmane, Malik,$$eauthor.
000720623 24510 $$aRift-lines within European regulatory framework for biosimilars when taking heterogeneity and variation during lifecycle of the reference biologic and the biosimilar into account$$h[electronic resource] /$$cMalik Osmane.
000720623 264_1 $$aHamburg, Germany :$$bAnchor Academic Publishing,$$c2014.
000720623 264_4 $$c©2014
000720623 300__ $$a1 online resource (283 pages) :$$billustrations (some color)
000720623 336__ $$atext$$2rdacontent
000720623 337__ $$acomputer$$2rdamedia
000720623 338__ $$aonline resource$$2rdacarrier
000720623 504__ $$aIncludes bibliographical references.
000720623 506__ $$aAccess limited to authorized users.
000720623 588__ $$aDescription based on online resource; title from PDF cover (ebrary, viewed April 15, 2014).
000720623 650_0 $$aBiological products.
000720623 650_0 $$aDrugs$$xGeneric substitution.
000720623 650_0 $$aPharmaceutical biotechnology industry.
000720623 77608 $$iPrint version:$$aOsmane, Malik.$$tRift-lines within European regulatory framework for biosimilars when taking heterogeneity and variation during lifecycle of the reference biologic and the biosimilar into account.$$dHamburg, Germany : Anchor Academic Publishing, c2014 $$z9783954891870
000720623 852__ $$bebk
000720623 85640 $$3ProQuest Ebook Central Academic Complete$$uhttps://univsouthin.idm.oclc.org/login?url=http://site.ebrary.com/lib/usiricelib/Doc?id=10856569$$zOnline Access
000720623 909CO $$ooai:library.usi.edu:720623$$pGLOBAL_SET
000720623 980__ $$aEBOOK
000720623 980__ $$aBIB
000720623 982__ $$aEbook
000720623 983__ $$aOnline