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Num Mark Titles (251-300 of 337) Year Entries
371 Found
251 Guidance for industry [electronic resource] : questions and answers regarding food allergens, includ   2006 1
252 Guidance for industry [electronic resource] : recognition and use of a standard for uniform blood an   2006 1
253 Guidance for industry [electronic resource] : recommendations for assessment of donor suitability an   2001 1
254 Guidance for industry [electronic resource] : recommendations for collecting red blood cells by auto   2001 1
255 Guidance for industry [electronic resource] : recommendations for deferral of donors and quarantine   2002 1
256 Guidance for industry [electronic resource] : recommendations for donor questioning regarding possib   2000 1
257 Guidance for industry [electronic resource] : recommendations for obtaining a labeling claim for com   2004 1
258 Guidance for industry [electronic resource] : regulation of human cells, tissues, and cellular and t   2007 1
259 Guidance for industry [electronic resource] : reports on the status of postmarketing study commitme   2006 1
260 Guidance for industry [electronic resource] : requalification method for reentry of blood donors def   2008 1
261 Guidance for industry [electronic resource] : residual solvents in drug products marketed in the Uni   2009 1
262 Guidance for industry [electronic resource] : revised preventive measures to reduce the possible ris   2002 1
263 Guidance for industry [electronic resource] : revised recommendations for donor and product manageme   2003 1
264 Guidance for industry [electronic resource] : revised recommendations for the assessment of donor su   2003 1
265 Guidance for industry [electronic resource] : revised recommendations regarding invalidation of test   2001 1
266 Guidance for industry [electronic resource] : revising and ANDA labeling following revision of the R   2000 1
267 Guidance for industry [electronic resource] : S1B testing for carcinogenicity of pharmaceuticals.   1997 1
268 Guidance for industry [electronic resource] : S1C(R2) dose selection for carcinogenicity studies.   2008 1
269 Guidance for industry [electronic resource] : S2B genotoxicity, a standard battery for genotoxicity   1997 1
270 Guidance for industry [electronic resource] : S6 preclinical safety evaluation of biotechnology-deri   1997 1
271 Guidance for industry [electronic resource] : S7A safety pharmacology studies for human pharmaceutic   2001 1
272 Guidance for industry [electronic resource] : S7B nonclinical evaluation of the potential for delaye   2005 1
273 Guidance for industry [electronic resource] : S8 immunotoxicity studies for human pharmaceuticals.   2006 1
274 Guidance for industry [electronic resource] : safety, efficacy, and pharmacokinetic studies to suppo   2008 1
275 Guidance for industry [electronic resource] : safety studies for veterinary drug residues in human f   2006 1
276 Guidance for industry [electronic resource] : safety testing of drug metabolites.   2008 1
277 Guidance for industry [electronic resource] : single dose acute toxicity testing for pharmaceuticals   1996 1
278 Guidance for industry [electronic resource] : somatic cell therapy for cardiac disease.   2009 1
279 Guidance for industry [electronic resource] : source animal, product, preclinical, and clinical issu   2003 1
280 Guidance for industry [electronic resource] : SPL standard for content of labeling technical Qs & As   2009 1
281 Guidance for industry [electronic resource] : stability testing for medicated premixes.   2000 1
282 Guidance for industry [electronic resource] : stability testing of new biotechnological/biological v   2001 1
283 Guidance for industry [electronic resource] : stability testing of new veterinary dosage forms.   1999 1
284 Guidance for industry [electronic resource] : stability testing of new veterinary drug substances an   1999 1
285 Guidance for industry [electronic resource] : stability testing, photostability testing of new veter   1999 1
286 Guidance for industry [electronic resource] : standards for securing the drug supply chain : standar   2009 1
287 Guidance for industry [electronic resource] : statistical approaches to establishing bioequivalence.   2001 1
288 Guidance for industry [electronic resource] : sterile drug products produced by aseptic processing,   2004 1
289 Guidance for industry [electronic resource] : streamlining the donor interview process, recommendati   2003 1
290 Guidance for industry [electronic resource] : street drug alternatives.   2000 1
291 Guidance for industry [electronic resource] : studies to evaluate the safety of residues of veterina   2006 1
292 Guidance for industry [electronic resource] : studies to evaluate the safety of residues of veterina   2006 1
293 Guidance for industry [electronic resource] : submission of documentation in applications for parame   2
294 Guidance for industry [electronic resource] : submitting marketing applications according to the ICH   2001 1
295 Guidance for industry [electronic resource] : submitting type V drug master files to the Center for   2001 1
296 Guidance for industry [electronic resource] : SUPAC-IR/MR : immediate release and modified release s   1999 1
297 Guidance for industry [electronic resource] : SUPAC-MR : modified release solid oral dosage forms :   1997 1
298 Guidance for industry [electronic resource] : SUPAC-SS : nonsterile semisolid dosage forms : manufac   1998 1
299 Guidance for industry [electronic resource] : supplemental guidance on testing for replication compe   2006 1
300 Guidance for industry [electronic resource] : supplemental testing and the notification of consignee   1998 1
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