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

Title 21 CFR Part 11
Results: 594

#	Item
11	JUNE 2, 2015 MEDICAL DEVICE INNOVATION CONSORTIUM (MDIC) CLINICAL TRIAL INNOVATION AND REFORM PROJECT REPORT Add to Reading List Source URL: mdic.org Language: English - Date: 2015-06-04 11:27:01 Food and Drug Administration Pharmaceutical industry Design of experiments United States administrative law Clinical trial Product testing Title 21 CFR Part 11 Institutional review board Public Responsibility in Medicine and Research Medical device
12	This document is scheduled to be published in the Federal Register onand available online at http://federalregister.gov/a, and on FDsys.govP DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: s3.amazonaws.com Language: English - Date: 2015-05-05 08:45:34 Technology Medical device Premarket approval Validation Direct-to-consumer advertising Federal Food Drug and Cosmetic Act Title 21 CFR Part 11 Structured Product Labeling Medicine Food and Drug Administration Health
13	Microsoft Word - SPCC_Draft_5.24.11 Add to Reading List Source URL: www.cheyenneairport.com Language: English - Date: 2011-10-05 12:25:45 Pharmaceuticals policy Title 21 CFR Part 11 United States federal law Medicine Government Technology United States administrative law Food and Drug Administration Pharmaceutical industry
14	Pharma Electronic Signatures and Audit Trail FDA 21 CFR Part II Compliant The Industry Standard System for Add to Reading List Source URL: www.iccs-ltd.co.uk Language: English - Date: 2014-11-19 10:20:43 Pharmacology Pharmaceutics Validity Clinical research Quality Validation Title 21 CFR Part 11 Electronic signature Good Automated Manufacturing Practice Pharmaceutical industry Pharmaceutical sciences Pharmaceuticals policy
15	ClientAlert June 24, 2013 Berwyn \| Boston \| Detroit \| Harrisburg \| Los Angeles \| New York \| Orange County \| Philadelphia \| Pittsburgh \| Princeton \| Washington, D.C. \| Wilmington Unhack My Heart: FDA Issues Guidance to M Add to Reading List Source URL: www.aamc.org Language: English - Date: 2014-07-23 10:45:45 Health Medical device Premarket approval Computer security Title 21 CFR Part 11 Center for Devices and Radiological Health Medicine Food and Drug Administration Technology
16	Federal Register / Vol. 80, NoMonday, March 9, Notices time. Persons who do not file an advance request for a presentation, but Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-03-09 13:45:46 Health Pharmacology Pharmaceutical industry Pharmaceuticals policy Institutional review board Office for Human Research Protections Food and Drug Administration Title 21 of the Code of Federal Regulations Title 21 CFR Part 11 Medicine Clinical research Research
17	BFMA Symposium 2002 May 23, 8:00-9:30 AM - #62 The Evolution of E-Forms & E-SIGN Barclay T. Blair Add to Reading List Source URL: www.kahnconsultinginc.com Language: English - Date: 2007-06-06 22:46:00 Electronic signature Uniform Electronic Transactions Act Digital signature Government Paperwork Elimination Act Electronic Signatures in Global and National Commerce Act MERS Title 21 CFR Part 11 Signature Time signature Cryptography Law Computer law
18	Federal Register / Vol. 80, NoMonday, March 9, Notices Ave., Bldg. 32, Rm. 5103, Silver Spring, MD 20993–0002; or the Office of Communication, Outreach and Development, Center for Biologics Evaluation and Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-03-09 13:45:44 Health Pharmacology Food and Drug Administration Pharmaceutical industry Design of experiments Institutional review board Office for Human Research Protections Title 21 CFR Part 11 Regulatory requirement Clinical research Research Medicine
19	Federal Register / Vol. 76, NoThursday, July 7, Unified Agenda Appendix A—Instructions for Obtaining Copies of Regulatory Documents Appendix B—General Rulemaking Contact Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-05-23 10:53:06 Law Federal Register Code of Federal Regulations Title 21 CFR Part 11 Rulemaking Regulatory Flexibility Act Government procurement in the United States Federal Acquisition Regulation United States administrative law Government Politics of the United States
20	Microsoft Word - SL-AN-27.doc Add to Reading List Source URL: www.microtrac.net Language: English - Date: 2012-10-02 14:12:51 Food and Drug Administration Pharmaceuticals policy Title 21 CFR Part 11 Law Government Electronic signature Technology Password Adobe Flex Pharmaceutical industry Computer law Cryptography