000 01275 a2200325 4500
005 20250516011357.0
264 0 _c20110923
008 201109s 0 0 eng d
022 _a1872-8294
024 7 _a10.1016/j.addr.2010.10.010
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMuller, Patrick Y
245 0 0 _aComparative requirements for exploratory clinical trials -- eIND, eCTA and microdosing.
_h[electronic resource]
260 _bAdvanced drug delivery reviews
_cJun 2011
300 _a511-7 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAnimals
650 0 4 _aAntibodies, Monoclonal
_xadministration & dosage
650 0 4 _aBiotechnology
_xmethods
650 0 4 _aClinical Trials as Topic
_xlegislation & jurisprudence
650 0 4 _aClinical Trials, Phase I as Topic
_xlegislation & jurisprudence
650 0 4 _aDose-Response Relationship, Drug
650 0 4 _aDrugs, Investigational
_xadministration & dosage
650 0 4 _aGuidelines as Topic
650 0 4 _aHumans
650 0 4 _aInternational Cooperation
650 0 4 _aModels, Biological
773 0 _tAdvanced drug delivery reviews
_gvol. 63
_gno. 7
_gp. 511-7
856 4 0 _uhttps://doi.org/10.1016/j.addr.2010.10.010
_zAvailable from publisher's website
999 _c20334657
_d20334657