Drugs -- Testing
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The concept Drugs -- Testing represents the subject, aboutness, idea or notion of resources found in University of Missouri-St. Louis Libraries.
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Drugs -- Testing
Resource Information
The concept Drugs -- Testing represents the subject, aboutness, idea or notion of resources found in University of Missouri-St. Louis Libraries.
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- Drugs -- Testing
53 Items that share the Concept Drugs -- Testing
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- Addendum to ICH S6 : preclinical safety evaluation of biotechnology-derived pharmaceuticals
- Animal experiments in pharmacological analysis
- CDC trials of daily oral tenofovir for preventing HIV infection : phase II and III clinical trials in Botswana, Thailand and the United States
- Drug discovery and design : medical aspects
- Drugs and laboratory parameters
- Drugs and laboratory parameters
- El proceso del desarrollo de las drogas y la FDA : cómo la agencia asegura que las drogas sean seguras y efectivas
- Ensayos voluntarios de tratamientos médicos en clínicas experimentales
- FDA and the drug development process : how the agency ensures that drugs are safe and effective
- FDA fast track and priority review programs
- FDA-approved bargain drugs : generic products must meet high standards
- Food and Drug Administration : FDA faces challenges meeting its growing medical product responsibilities and should develop complete estimates of its resource needs : report to congressional requesters
- Guidance for industry : CGMP for phase 1 investigational drugs
- Guidance for industry : E 11 clinical investigation of medicinal products in the pediatric population
- Guidance for industry : E14 clinical evaluation of QT/QTc interval prolongation and proarrhythmic potential for non-antiarrhythmic drugs
- Guidance for industry : E2B(M), data elements for transmission of individual case study reports, questions and answers
- Guidance for industry : E2BM data elements for transmission of individual case safety reports
- Guidance for industry : M3 nonclinical safety studies for the conduct of human clinical trials for pharmaceuticals
- Guidance for industry : Q1A(R2) stability testing of new drug substances and products
- Guidance for industry : Q1D bracketing and matrixing designs for stability testing of new drug substances and products
- Guidance for industry : Q3C impurities, residual solvents
- Guidance for industry : S1B testing for carcinogenicity of pharmaceuticals
- Guidance for industry : S6 preclinical safety evaluation of biotechnology-derived pharmaceuticals
- Guidance for industry : S7B nonclinical evaluation of the potential for delayed ventricular repolarization (QT Interval Prolongation) by human pharmaceuticals
- Guidance for industry : S8 immunotoxicity studies for human pharmaceuticals
- Guidance for industry : addendum to E2C clinical safety data management : periodic safety update reports for marketed drugs
- Guidance for industry : drug-induced liver injury, premarketing clinical evaluation
- Guidance for industry : estimating the maximum safe starting dose in initial clinical trials for therapeutics in adult healthy volunteers
- Guidance for industry : process validation, general principles and practices
- Guidance for industry : tropical disease priority review vouchers
- Guidance on nonclinical safety studies for the conduct of human clinical trials and marketing authorization for pharmaceuticals
- Handbook for clinical investigators
- Human-based systems for translational research
- Improving and accelerating therapeutic development for nervous system disorders : workshop summary
- Improving and accelerating therapeutic development for nervous system disorders : workshop summary
- Improving public health : promting safe and effective drug use
- Las drogas baratas aprobadas por la FDA : los productos genéricos deben satisfacer altos niveles
- Manual del Centro para la Evaluacion e Investigacion de Farmacos
- Mejorando la salud pública : fomentando la venta y el uso de drogas efectivas
- Monitoring for drug safety
- Pediatric drug research : Food and Drug Administration should more efficiently monitor inclusion of minority children
- Pharmacokinetics : guidance for repeated dose tissue distribution studies
- Prescription drugs : FDA guidance and regulations related to data on elderly persons in clinical drug trials
- Prostate Cancer Prevention Trial (PCPT)
- Reforming the FDA
- Revision of the ICH guideline on clinical safety data management : data elements for transmission of individual case safety reports
- S2(R1) genotoxicity testing and data interpretation for pharmaceuticals intended for human use
- Successfully marketing clinical trial results : winning in the healthcare business
- Successfully marketing clinical trial results : winning in the healthcare business
- Target validation in drug discovery
- Virtual clinical trials : challenges and opportunities : proceedings of a workshop
- Visita radial a ClinicalTrials.gov : preguntas y respuestas
- Why volunteer? : clinical trials of medical treatments
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<div class="citation" vocab="http://schema.org/"><i class="fa fa-external-link-square fa-fw"></i> Data from <span resource="http://link.umsl.edu/resource/r0y3K_Q_lXs/" typeof="CategoryCode http://bibfra.me/vocab/lite/Concept"><span property="name http://bibfra.me/vocab/lite/label"><a href="http://link.umsl.edu/resource/r0y3K_Q_lXs/">Drugs -- Testing</a></span> - <span property="potentialAction" typeOf="OrganizeAction"><span property="agent" typeof="LibrarySystem http://library.link/vocab/LibrarySystem" resource="http://link.umsl.edu/"><span property="name http://bibfra.me/vocab/lite/label"><a property="url" href="http://link.umsl.edu/">University of Missouri-St. Louis Libraries</a></span></span></span></span></div>
