Food and Drug Administration - PDFSEARCH.IO - Document Search Engine

Food and Drug Administration
Results: 36271

#	Item
431	SOP 24 - OHSRP REPORTING TO THE OFFICE FOR HUMAN RESEARCH PROTECTIONS (OHSRP) AND THE FOOD AND DRUG ADMINISTRATION (FDA) REGARDING UNANTICIPATED PROBLEMS, SERIOUS OR CONTINUING NONCOMPLIANCE, OR TERMINATIONS OR SUSPENSIO Add to Reading List Source URL: ohsr.od.nih.gov Language: English - Date: 2015-09-29 17:00:19
432	See Does My Project Need IRB Review? If there is any question whether your project is human subject research you must submit this form to the IRB. Complete all sections then email to . Th Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-01-27 16:54:35 Clinical research Pharmaceutical industry Medical ethics Design of experiments Human subject research Clinical trial Office for Human Research Protections Food and Drug Administration Public Responsibility in Medicine and Research Clinical research coordinator
433	IIB 114TH CONGRESS 1ST SESSION H. R. 1599 Add to Reading List Source URL: www.congress.gov Language: English - Date: 2015-07-28 05:24:14 Food and Drug Administration Environment Plant Protection Act United States Department of Agriculture Emerging technologies Molecular biology Federal Food Drug and Cosmetic Act Genetic engineering
434	ASSOCIATION FOR MOLECULAR PATHOLOGY Education. Innovation & Improved Patient Care. Advocacy. 9650 Rockville Pike. Bethesda, Maryland 20814 Tel: 301‐634‐7939 \| Fax: 301‐634‐7995 Add to Reading List Source URL: www.amp.org Language: English - Date: 2015-08-04 16:38:18 Medicine Health Biology Medical diagnosis Medical technology Biotechnology Molecular diagnostics Clinical Laboratory Improvement Amendments Medical laboratory Food and Drug Administration Pathology
435	June 30, 2015 Dr. Steven Ostroff Acting Commissioner Food and Drug Administration (FDANew Hampshire Avenue Silver Spring, MD 20993 Add to Reading List Source URL: www.gphaonline.org Language: English - Date: 2015-06-30 09:54:35
436	Society(for(Science,Based(Medicine( ! Comment:((Homeopathic(Product(Regulation:(Evaluating(the(Food( and(Drug(Administration’s(Regulatory(Framework(After(a(Quarter, Century( ( Add to Reading List Source URL: sfsbm.org Language: English - Date: 2015-08-23 16:11:11
437	Proposal for Modernization of CLIA Regulations for Laboratory Developed Testing Procedures (LDPs) Transparency. Quality. Innovation. Desired Outcomes: • Patients receive the most appropriate test(s) for their clinical Add to Reading List Source URL: www.amp.org Language: English - Date: 2015-08-17 17:19:34 Health Medical research Laboratories Clinical Laboratory Improvement Amendments Health in the United States Safety Medical technology Medical laboratory Clinical trial Food and Drug Administration Protocol
438	Content of Premarket Submissions for Management of Cybersecurity in Medical Devices Guidance for Industry and Food and Drug Administration Staff Document Issued on: October 2, 2014 Add to Reading List Source URL: www.fda.gov Language: English Health Prevention Security Food and Drug Administration Cyberwarfare Medical technology Medical device Medical equipment Pharmaceuticals policy Risk management Computer security Control system security
439	Minutes of NRSP-7 Spring Annual Meeting 2008 st nd April 21 and 22 , 2008 LOCATION: U. S. Food and Drug Administration Center for Veterinary Medicine Add to Reading List Source URL: www.nrsp-7.org Language: English - Date: 2008-06-16 13:36:50
440	An organization’s employees or agents refers to individuals who: (1) act on behalf of the institution; (2) exercise institutional authority or responsibility; or (3) perform institutionally designated activities. “E Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2013-05-07 11:04:12 Medical research Research Health Clinical research Medical ethics Research ethics Design of experiments Clinical trial Human subject research Food and Drug Administration Informed consent

UPDATE