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Num Mark 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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