000 01559 a2200421 4500
005 20250515080155.0
264 0 _c20071213
008 200712s 0 0 eng d
022 _a0360-3016
024 7 _a10.1016/j.ijrobp.2007.04.054
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDavidson, Susan E
245 0 0 _aImproving the capture of adverse event data in clinical trials: the role of the International Atomic Energy Agency.
_h[electronic resource]
260 _bInternational journal of radiation oncology, biology, physics
_cNov 2007
300 _a1218-21 p.
_bdigital
500 _aPublication Type: Congress
650 0 4 _aClinical Trials as Topic
_xstandards
650 0 4 _aColorado
650 0 4 _aData Collection
_xmethods
650 0 4 _aDrug-Related Side Effects and Adverse Reactions
650 0 4 _aHumans
650 0 4 _aInternational Agencies
650 0 4 _aNational Cancer Institute (U.S.)
_xstandards
650 0 4 _aNuclear Energy
650 0 4 _aObserver Variation
650 0 4 _aRadiotherapy
_xadverse effects
650 0 4 _aSurveys and Questionnaires
_xstandards
650 0 4 _aTerminology as Topic
650 0 4 _aUnited States
700 1 _aTrotti, Andy
700 1 _aAtaman, Ozlem U
700 1 _aSeong, Jinsil
700 1 _aLau, Fen Nee
700 1 _ada Motta, Neiro W
700 1 _aJeremic, Branislav
773 0 _tInternational journal of radiation oncology, biology, physics
_gvol. 69
_gno. 4
_gp. 1218-21
856 4 0 _uhttps://doi.org/10.1016/j.ijrobp.2007.04.054
_zAvailable from publisher's website
999 _c17220841
_d17220841