000 01940nam a2200397 i 4500
001 ebr10856569
003 CaPaEBR
007 cr cn|||||||||
008 140416t20142014gw a ob 000 0 eng d
020 _z9783954891870
020 _z9783954896875 (PDF)
040 _aCaPaEBR
_beng
_erda
_epn
_cCaPaEBR
035 _a(OCoLC)878147377
050 1 4 _aRS189
_b.O863 2014eb
082 0 4 _a572
_223
100 1 _aOsmane, Malik,
_eauthor.
245 1 0 _aRift-lines within European regulatory framework for biosimilars when taking heterogeneity and variation during lifecycle of the reference biologic and the biosimilar into account /
_cMalik Osmane.
264 1 _aHamburg, Germany :
_bAnchor Academic Publishing,
_c2014.
264 4 _c�2014
300 _a1 online resource (283 pages) :
_billustrations (some color)
336 _atext
_2rdacontent
337 _acomputer
_2rdamedia
338 _aonline resource
_2rdacarrier
504 _aIncludes bibliographical references.
588 _aDescription based on online resource; title from PDF cover (ebrary, viewed April 15, 2014).
590 _aElectronic reproduction. Palo Alto, Calif. : ebrary, 2014. Available via World Wide Web. Access may be limited to ebrary affiliated libraries.
650 0 _aBiological products.
650 0 _aDrugs
_xGeneric substitution.
650 0 _aPharmaceutical biotechnology industry.
655 0 _aElectronic books.
776 0 8 _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
_h12 pages
_z9783954891870
797 2 _aebrary.
856 4 0 _uhttp://site.ebrary.com/lib/kliuc/Doc?id=10856569
_zAn electronic book accessible through the World Wide Web; click to view
942 _2lcc
_cEBK
999 _c186532
_d186532