000 01376 a2200337 4500
005 20250514223824.0
264 0 _c20051110
008 200511s 0 0 ger d
022 _a1436-9990
024 7 _a10.1007/s00103-005-1015-8
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHeidenreich, K
245 0 0 _a[Clinical trials in Germany and in the EU in the new legislative environment. An analysis from the industry's point of view].
_h[electronic resource]
260 _bBundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
_cApr 2005
300 _a415-22 p.
_bdigital
500 _aPublication Type: English Abstract; Journal Article
650 0 4 _aClinical Trials as Topic
_xlegislation & jurisprudence
650 0 4 _aDrug Approval
_xlegislation & jurisprudence
650 0 4 _aDrug-Related Side Effects and Adverse Reactions
650 0 4 _aEuropean Union
650 0 4 _aGermany
650 0 4 _aGuidelines as Topic
650 0 4 _aHumans
650 0 4 _aMulticenter Studies as Topic
650 0 4 _aQuality Assurance, Health Care
_xlegislation & jurisprudence
700 1 _aMöritz, A
700 1 _aLöffler, H
700 1 _aOberle-Rolle, B
773 0 _tBundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
_gvol. 48
_gno. 4
_gp. 415-22
856 4 0 _uhttps://doi.org/10.1007/s00103-005-1015-8
_zAvailable from publisher's website
999 _c15498814
_d15498814