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Titles (101-150 of 337)
Year
Entries
371 Found
101
Guidance for industry [electronic resource] : E 11 clinical investigation of medicinal products in t
2000
1
102
Guidance for industry [electronic resource] : E14 clinical evaluation of QT/QTc interval prolongatio
2
103
Guidance for industry [electronic resource] : E15 definitions for genomic biomarkers, pharmacogenomi
2008
1
104
Guidance for industry [electronic resource] : E2B(M), data elements for transmission of individual c
2005
1
105
Guidance for industry [electronic resource] : E2BM data elements for transmission of individual case
2002
1
106
Guidance for industry [electronic resource] : E2E pharmacovigilance planning.
2005
1
107
Guidance for industry [electronic resource] : E6 good clinical practice, consolidated guidance.
2000
1
108
Guidance for industry [electronic resource] : E9 statistical principles for clinical trials.
1998
1
109
Guidance for industry [electronic resource] : effectiveness of anthelmintics, general recommendation
2001
1
110
Guidance for industry [electronic resource] : effectiveness of anthelmintics, specific recommendatio
2001
1
111
Guidance for industry [electronic resource] : effectiveness of anthelmintics, specific recommendatio
2001
1
112
Guidance for industry [electronic resource] : effectiveness of anthelmintics, specific recommendatio
2002
1
113
Guidance for industry [electronic resource] : effectiveness of anthelmintics, specific recommendatio
2002
1
114
Guidance for industry [electronic resource] : effectiveness of anthelmintics, specific recommendatio
2001
1
115
Guidance for industry [electronic resource] : effectiveness of anthelmintics, specific recommendatio
2002
1
116
Guidance for industry [electronic resource] : effectiveness of anthelmintics, specific recommendatio
2002
1
117
Guidance for industry [electronic resource] : efficacy studies to support marketing of fibrin sealan
1999
1
118
Guidance for industry [electronic resource] : eligibility determination for donors of human cells, t
2007
1
119
Guidance for industry [electronic resource] : environmental assessment of human drug and biologics a
1998
1
120
Guidance for industry [electronic resource] : environmental impact assessments (EIA's) for veterinar
2001
1
121
Guidance for industry [electronic resource] : errors and accidents regarding saline dilution of samp
1998
1
122
Guidance for industry [electronic resource] : estimating the maximum safe starting dose in initial c
2005
1
123
Guidance for industry [electronic resource] : expiration dating and stability testing of solid oral
1997
1
124
Guidance for industry [electronic resource] : exports under the FDA Export Reform and Enhancement Ac
2007
1
125
Guidance for industry [electronic resource] : extended release oral dosage forms, development, evalu
1997
1
126
Guidance for industry [electronic resource] : fast track drug development programs, designation, dev
2
127
Guidance for industry [electronic resource] : FDA export certificates.
2005
1
128
Guidance for industry [electronic resource] : FDA review of vaccine labeling requirements for warnin
2004
1
129
Guidance for industry [electronic resource] : financial disclosure by clinical investigators.
2001
1
130
Guidance for industry [electronic resource] : food-effect bioavailability and fed bioequivalence stu
2002
1
131
Guidance for industry [electronic resource] : formal dispute resolution, appeals above the division
2000
1
132
Guidance for industry [electronic resource] : formal dispute resolution : scientific and technical i
2006
1
133
Guidance for industry [electronic resource] : formal meetings between the FDA and sponsors or applic
2009
1
134
Guidance for industry [electronic resource] : format and content for the CMC section of an annual re
1994
1
135
Guidance for industry [electronic resource] : gene therapy clinical trials, observing subjects for d
2006
1
136
Guidance for industry [electronic resource] : general principles for the development of vaccines to
2008
1
137
Guidance for industry [electronic resource] : good pharmacovigilance practices and pharmacoepidemiol
2005
1
138
Guidance for industry [electronic resource] : granularity document : annex to M4, organization of th
2005
1
139
Guidance for industry [electronic resource] : guidance for human somatic cell therapy and gene thera
1998
1
140
Guidance for industry [electronic resource] : guidance on the labeling of certain uses of Lecithin d
2006
1
141
Guidance for industry [electronic resource] : handling and retention of BA and BE testing samples.
2004
1
142
Guidance for industry [electronic resource] : how to complete the vaccine adverse event reporting sy
1998
1
143
Guidance for industry [electronic resource] : how to comply with the Pediatric Research Equity Act.
2005
1
144
Guidance for industry [electronic resource] : hypertension indication, drug labeling for cardiovascu
2008
1
145
Guidance for industry [electronic resource] : immunotoxicology evaluation of investigational new dru
2002
1
146
Guidance for industry [electronic resource] : implementation of acceptable full-length donor history
2006
1
147
Guidance for industry [electronic resource] : implementation of Section 126 of the Food and Drug Adm
1998
1
148
Guidance for industry [electronic resource] : implementing a collection program for source plasma co
2006
1
149
Guidance for industry [electronic resource] : impurities in new veterinary drug substances (revision
2007
1
150
Guidance for industry [electronic resource] : impurities, residual solvents in new veterinary medici
2001
1
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