000 01632 a2200421 4500
005 20250516030820.0
264 0 _c20110930
008 201109s 0 0 eng d
022 _a1879-0720
024 7 _a10.1016/j.ejps.2011.03.004
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGiordani, Antonio
245 0 0 _aOverall impact of the regulatory requirements for genotoxic impurities on the drug development process.
_h[electronic resource]
260 _bEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
_cMay 2011
300 _a1-15 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAnimals
650 0 4 _aChemistry, Pharmaceutical
650 0 4 _aDNA Damage
650 0 4 _aDrug Contamination
_xlegislation & jurisprudence
650 0 4 _aDrug Industry
_xstandards
650 0 4 _aEurope
650 0 4 _aGuidelines as Topic
650 0 4 _aHumans
650 0 4 _aInternational Cooperation
650 0 4 _aMice
650 0 4 _aMutagens
_xanalysis
650 0 4 _aPharmaceutical Preparations
_xanalysis
650 0 4 _aQuality Control
650 0 4 _aRisk Assessment
650 0 4 _aToxicity Tests
_xstandards
650 0 4 _aUnited States
650 0 4 _aUnited States Food and Drug Administration
700 1 _aKobel, Werner
700 1 _aGally, Hans Ulrich
773 0 _tEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
_gvol. 43
_gno. 1-2
_gp. 1-15
856 4 0 _uhttps://doi.org/10.1016/j.ejps.2011.03.004
_zAvailable from publisher's website
999 _c20690945
_d20690945