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Clinical study design
Results: 811

#	Item
711	WHAT WORKS CLEARINGHOUSE REGISTRY OF RANDOMIZED CONTROLLED TRIALS REGISTRATION FORM Thank you for choosing to register a study for the What Works Clearinghouse Registry of Randomized Controlled Trials (RCTs). Please note Add to Reading List Source URL: ies.ed.gov Language: English - Date: 2012-07-17 16:04:38 Knowledge Clinical research Design of experiments Epidemiology Nursing research Randomized controlled trial Clinical trial Statistics Impact evaluation Science Information Evaluation methods
712	October 2012 Disclaimer: The following information is fictional and is only intended for the purposes of illustrating key concepts for results data entry in the Protocol Registration System (PRS). Example Parallel Study Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-03-11 16:44:01 Research Pharmacology Bioethics Medical ethics Design of experiments Placebo Clinical trial Pain Tapentadol Clinical research Medicine Science
713	Azelastine N22-203S008 Statistical PREA Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Research Bioethics Medical ethics Design of experiments Azelastine Placebo-controlled study Placebo Clinical trial Medicine Science Clinical research
714	N21-436S036 Aripiprazole Clinical PREA Add to Reading List Source URL: www.fda.gov Language: English Research Medicine Design of experiments Evaluation methods Bioethics Aripiprazole Placebo-controlled study Clinical trial Placebo Clinical research Science Pharmacology
715	Guidance for Industry E 10 Choice of Control Group and Related Issues in Clinical Trials U.S. Department of Health and Human Services Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Research Scientific method Pharmacology Pharmaceutical industry Evaluation methods Clinical trial Placebo-controlled study Assay sensitivity Placebo Clinical research Science Design of experiments
716	Guidance for Industry Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmaceutical industry Design of experiments Clinical trial Institutional review board Clinical investigator Good Clinical Practice Food and Drug Administration ClinicalTrials.gov Clinical research Research Science
717	Specifications for Preparing and Submitting Summary Level Clinical Site Data for CDER’s Inspection Planning Add to Reading List Source URL: www.fda.gov Language: English Science Food and Drug Administration Design of experiments Evaluation methods Pharmacology Electronic Common Technical Document Clinical trial Placebo-controlled study Investigational New Drug Research Clinical research Medicine
718	Guidance for Industry and FDA Staff Preparing Notices of Availability of Investigational Medical Devices and for Recruiting Study Subjects Good Guidance Practice Level 2 Document issued on: March 19, 1999 Add to Reading List Source URL: www.fda.gov Language: English Health Pharmacology Pharmaceutical industry Food and Drug Administration Design of experiments Investigational Device Exemption Clinical trial Clinical investigator Institutional review board Clinical research Medicine Research
719	Guidance for Industry Exposure-Response Relationships — Study Design, Data Analysis, and Regulatory Applications U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English Pharmacokinetics Clinical research Toxicology Design of experiments Dose-response relationship Bioequivalence Bioavailability Methadone Clinical trial Pharmaceutical sciences Pharmacology Medicine
720	N21-797S018 Entecavir Statistical BPCA Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Research Bioethics Medical ethics Design of experiments Entecavir Hepatitis B Placebo-controlled study Placebo Medicine Science Clinical research

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