Title 21 CFR Part 11 - PDFSEARCH.IO - Document Search Engine

Title 21 CFR Part 11
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41	Microsoft Word[removed][removed]pi.docx Add to Reading List Source URL: www.ofr.gov Language: English - Date: 2015-02-10 07:17:58 Technology Medical device Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Unique Device Identification Title 21 CFR Part 11 Food and Drug Administration Medicine Health
42	foSU.V1l:$ofJ (-~:1 -l MEMORANDUM Add to Reading List Source URL: lasikcomplications.com Language: English - Date: 2009-06-10 21:38:09 Pharmaceutical sciences Center for Devices and Radiological Health Medical device Premarket approval Regulatory requirement Adverse event Criticism of the Food and Drug Administration Title 21 CFR Part 11 Food and Drug Administration Medicine Health
43	Use of Electronic Informed Consent in Clinical Investigations Questions and Answers Guidance for Industry DRAFT GUIDANCE Add to Reading List Source URL: www.fda.gov Language: English Research Pharmaceutical industry Medical ethics Pharmacology Pharmaceuticals policy Institutional review board Title 21 CFR Part 11 Informed consent Validation Medicine Clinical research Health
44	Federal Register / Vol. 68, No[removed]Monday, March 31, [removed]Rules and Regulations 450 Fifth Street, NW, Washington, DC 20549–0312. SUPPLEMENTARY INFORMATION: I. Background On January 28, 2003, the Commission Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 22:45:19 Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry Food law Clinical research Federal Food Drug and Cosmetic Act Title 21 CFR Part 11 Title 21 of the Code of Federal Regulations Adverse event Food and Drug Administration Medicine Health
45	Federal Register / Vol. 68, No[removed]Monday, March 31, [removed]Rules and Regulations 450 Fifth Street, NW, Washington, DC 20549–0312. SUPPLEMENTARY INFORMATION: I. Background On January 28, 2003, the Commission Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 22:45:19 Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry Food law Clinical research Federal Food Drug and Cosmetic Act Title 21 CFR Part 11 Title 21 of the Code of Federal Regulations Adverse event Food and Drug Administration Medicine Health
46	QUALIFICATION GUIDELINE Qualification Guideline for Microsoft Azure June 2014 Qualification Guideline for Microsoft Azure Add to Reading List Source URL: download.microsoft.com Language: English - Date: 2014-06-12 14:32:08 Technology Quality Validation Validity Azure Services Platform Title 21 CFR Part 11 Azure Microsoft GxP Pharmaceutical industry Clinical research Computing
47	In Vitro Diagnostic (IVD) Device Studies; Draft Guidance for Industry and FDA Add to Reading List Source URL: www.upstate.edu Language: English - Date: 2009-12-11 15:24:18 Technology Pharmacology Pharmaceuticals policy Clinical research Pharmaceutical industry Investigational Device Exemption Medical device Title 21 CFR Part 11 Expanded access Medicine Food and Drug Administration Health
48	Information for Study Sponsors Add to Reading List Source URL: www.upstate.edu Language: English - Date: 2014-06-17 13:58:52 Medicine Science Design of experiments Pharmacology Drug safety Institutional review board Title 21 CFR Part 11 Adverse event Clinical research coordinator Clinical research Pharmaceutical industry Research
49	§ [removed]CFR Subtitle A (4–1–05 Edition) (b) As used in this part, residential structure includes the following: Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-12-29 13:59:08 Government procurement in the United States Office of Fair Housing and Equal Opportunity Government Accessibility Title 21 CFR Part 11 Politics of the United States United States administrative law Architectural Barriers Act Law
50	Microsoft Word - _82187764___6__Medical Device Update_ FDA Releases General Wellness Products and Device Accessories Guidances _final_.DOCX Add to Reading List Source URL: www.morganlewis.com Language: English - Date: 2015-01-28 10:22:16 Health Medical equipment Medical device Medical technology Wellness Title 21 CFR Part 11 Medicine Technology Food and Drug Administration

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