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020 _a0309218136
_q(pbk. : alk. paper)
020 _a0309218144
_q(PDF)
020 _a9780309218139
_q(pbk. : alk. paper)
020 _a9780309218146
_q(PDF)
040 _aDNLM/DLC
_beng
_cDLC
_dYDX
_dBTCTA
_dNLM
_dYDXCP
_dBWX
_dAAA
_dCDX
_dUN@
082 0 4 _a174.2951
_bE84 2012
245 1 0 _aEthical and scientific issues in studying the safety of approved drugs /
_cCommittee on Ethical and Scientific Issues in Studying the Safety of Approved Drugs, Board on Population Health and Public Health Practice, Institute of Medicine of the National Academies.
264 3 1 _aWashington, D.C. :
_bNational Academies Press,
_cc2012.
300 _axvi, 275 páginas :
_bilustraciones ;
_c23 cm.
336 _atexto
_btxt
_2rdacontent
337 _ano mediado
_bn
_2rdamedia
338 _avolumen
_bnc
_2rdacarrier
504 _aIncluye bibliografía.
505 0 _aIncorporating benefit and risk assessment and benefit/risk management into food and drug administration decision-making -- Evidence and decision-making -- Selection and oversight of required postmarketing studies -- Synthesis.
650 1 4 _9335324
_aMedicamentos.
_xPruebas
_xAspectos morales y éticos
_zEstados Unidos.
650 1 4 _9346898
_aPruebas clínicas.
_xAspectos morales y éticos
_zEstados Unidos.
710 2 _9148364
_aInstitute of Medicine (U.S.).
_bCommittee on Ethical and Scientific Issues in Studying the Safety of Approved Drugs.
942 _2ddc
_cGEN
991 _aC0
_bUN@
991 _aCB
_aPR13
_a000101358, Triana Contreras, Zeta Meva.
997 _aHZ
_b00
_c20140722
_lUDM01
_h1028
998 _aBATCH-UPD
_b00
_c20150424
_lUDM01
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999 _c132677
_d132677
900 _aADM
900 _aCC
900 _aCNT
900 _aCB