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Structured product
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#	Item
471	Promoting Regulated Products Lawfully Add to Reading List Source URL: www.jnj.com Language: English - Date: 2013-05-22 12:29:44 Pharmacology Pharmaceuticals policy Food and Drug Administration Clinical pharmacology United States Public Health Service Medical device Regulatory requirement Pharmaceutical industry Structured Product Labeling Medicine Health Pharmaceutical sciences
472	National Drug File – Reference Terminology (NDF-RT™) Documentation U.S. Department of Veterans Affairs, Veterans Health Administration March 2014 Version Add to Reading List Source URL: evs.nci.nih.gov Language: English - Date: 2014-03-04 10:54:27 Pharmaceutical sciences Pharmacology United States Department of Veterans Affairs Healthcare in the United States Structured Product Labeling Food and Drug Administration Abbreviated New Drug Application Veterans Health Administration Unified Medical Language System Health Medicine Medical informatics
473	JISC Shared Data centre product specification The Jisc shared data centre is a unique facility Add to Reading List Source URL: www.ja.net Language: English - Date: 2014-09-04 07:15:56 Electric power distribution Cloud storage Data center Data management Distributed data storage Networks Structured cabling Switchgear Rack unit Computing Electromagnetism Electrical engineering
474	FDA’s Home Use Medical Device Initiative Add to Reading List Source URL: www.fda.gov Language: English Technology Unique Device Identification Center for Devices and Radiological Health Medical device Premarket approval Adverse event Title 21 CFR Part 11 Structured Product Labeling Food and Drug Administration Medicine Health
475	Standardizing and Evaluating Risk Evaluation and Mitigation Strategies (REMS) Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmacy Food and Drug Administration Pharmaceuticals policy Medical informatics Prescription Drug User Fee Act Structured Product Labeling Pharmacovigilance Electronic prescribing Medicine Health Pharmaceutical sciences
476	Guidance for Industry Electronic Submission of Lot Distribution Reports DRAFT GUIDANCE This guidance document is for comment purposes only. Submit one set of either electronic or written comments on this draft guidance b Add to Reading List Source URL: www.fda.gov Language: English Research Structured Product Labeling Center for Biologics Evaluation and Research Adverse Event Reporting System Validation Electronic Common Technical Document Federal Food Drug and Cosmetic Act Abbreviated New Drug Application Title 21 CFR Part 11 Food and Drug Administration Medicine Health
477	September[removed]Guidelines on informing investors about structured products Introduction Add to Reading List Source URL: www.swissbanking.org Language: English - Date: 2014-09-10 05:11:54 Financial services Funds Securities Stock market Structured product Prospectus Credit rating agency Collateralized debt obligation Collective investment scheme Financial economics Investment Finance
478	The GUDID Account January 30, 2014 Indira R. Konduri GUDID Program Manager Add to Reading List Source URL: www.fda.gov Language: English Unique Device Identification Medical device Center for Devices and Radiological Health Structured Product Labeling Medicine Food and Drug Administration Health
479	Enhancing the National Drug File – Reference Terminology (NDF-RT) for Meaningful Use The Veterans Health Administration (VHA) National Drug File – Reference Terminology (NDF-RT) is a medication reference terminology Add to Reading List Source URL: evs.nci.nih.gov Language: English - Date: 2014-09-23 13:04:35 Medical informatics International standards Nursing informatics Electronic health record Structured Product Labeling Food and Drug Administration Daily Med Health information technology Alternative medicine Health Medicine Health informatics
480	Guidance for Industry Electronic Submission of Lot Distribution Reports DRAFT GUIDANCE This guidance document is for comment purposes only. Submit one set of either electronic or written comments on this draft guidance b Add to Reading List Source URL: www.fda.gov Language: English Research Structured Product Labeling Center for Biologics Evaluation and Research Adverse Event Reporting System Validation Electronic Common Technical Document Federal Food Drug and Cosmetic Act Abbreviated New Drug Application Title 21 CFR Part 11 Food and Drug Administration Medicine Health

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