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Clinical site
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#	Item
221	Clinical Trial Site Information Form Natural Health Products Directorate A separate form for each clinical trial site must be completed by the Sponsor and filed with Health Canada. All fields must be completed prior to Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:44 Science Clinical Data Management Clinical trial Clinical Trial Portal Clinical research coordinator Clinical research Research Pharmaceutical industry
222	UNMC RESEARCH QUICK REFERENCE – INDUSTRY-SPONSORED CLINICAL TRIALS & REGISTRIES ASSESS FEASIBILITY  Sponsor selects site  PI assesses feasibility: Add to Reading List Source URL: www.unmc.edu Language: English - Date: 2014-10-08 15:40:03 Science Design of experiments Pharmacology Pharmaceutical sciences Clinical trial Clinical research Pharmaceutical industry Research
223	FDA Patient Safety Initiative Update Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceutical industry pharmacology Clinical site Good Clinical Practice Food and Drug Administration Clinical investigator Clinical trial Center for Drug Evaluation and Research Research Clinical research Pharmaceutical sciences
224	Gonococcal Isolate Surveillance Project Form 1: Demographic /Clinical Data Sentinel Site: (3 letter code) Specimens collected during: Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2014-09-25 21:26:16 Medicine Thiazoles Otologicals Sexually transmitted diseases and infections Ceftriaxone Triazines Gonorrhea Azithromycin Cefpodoxime Piperazines Chemistry Organic chemistry
225	FOOD AND DRUG ADMINISTRATION PROGRAM[removed] Add to Reading List Source URL: www.fda.gov Language: English Research Pharmacology Food and Drug Administration Drug safety Bioequivalence Abbreviated New Drug Application Generic drug Clinical trial Clinical site Clinical research Pharmaceutical industry Pharmaceutical sciences
226	“Reporting Information Regarding Falsification of Data” Proposed Rule Add to Reading List Source URL: www.fda.gov Language: English pharmacology Pharmaceutics Good Clinical Practice Science Clinical investigator Sub-internship Clinical site Clinical trial Clinical research Pharmaceutical industry Research
227	The following is an outline of sections of the Manual of Operating Procedures (MOP) which should be considered for a multi-site study. However, given that each study is unique, sections could be omitted and/or added at t Add to Reading List Source URL: www.nia.nih.gov Language: English - Date: 2014-04-21 12:17:14 Health Insurance Portability and Accountability Act Privacy law Pharmaceutical industry Informed consent Law Research Health Clinical research Medical ethics Data privacy
228	QUalified investigator undeRtaking Natural Health Products Directorate Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:46 Science Food and Drug Administration Clinical trials Good Clinical Practice Clinical research coordinator Clinical site Clinical research Research Pharmaceutical industry
229	The following is an outline of sections of the Manual of Operating Procedures (MOP) which should be considered for a single-site study. However, given that each study is unique, sections could be omitted and/or added at Add to Reading List Source URL: www.nia.nih.gov Language: English - Date: 2014-04-21 12:17:25 Data privacy Health Insurance Portability and Accountability Act Privacy law Pharmaceutical industry Informed consent Law Scientific method Clinical research Medical ethics Research
230	Clinical Trial Site Information Form Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-09 13:04:27 Science Clinical trials Clinical Data Management Clinical Trial Portal Clinical research coordinator Clinical research Research Pharmaceutical industry

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