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Common Technical Document
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61	RTF Document Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:41 Clinical research Clinical data management Pharmaceutical industry Pharmaceuticals policy Electronic common technical document Common Technical Document Marketing authorization Validation Pharmacovigilance HTML element Summary of Product Characteristics European Medicines Agency
62	How to send submissions via the Web Client - User Guidance Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:47 Computer errors Digital media Research Clinical data management Electronic common technical document Form Electronic submission Email HTTP 404 Error message
63	PSUR Repository – MAH Training on new functionality Webinar training on new functionality provided in releasePresented by Kristiina Puusaari on 25 July 2016 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:01 Clinical data management Clinical research Electronic common technical document
64	Mandatory eCTD for Human centralised procedure ASMF submissions - Statement of Intent Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:57 Clinical research Clinical data management Electronic common technical document Digital media Research Common Technical Document
65	Supporting Document Mandatory Technical Document Evaluation Activities for Network Device cPP July-2016 Add to Reading List Source URL: www.commoncriteriaportal.org Language: English - Date: 2016-07-22 07:40:10 Cryptographic protocols Internet protocols World Wide Web Secure communication E-commerce HTTPS Hyperlink Public key certificate Password IPsec Common Criteria Hypertext Transfer Protocol
66	Q&A ON THE USE OF eCTD IN MRP/DCP Doc. Ref.:CMDhRev.23 JuneAprilHow to deal with National Translations of the Product Information Question 1.1 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-07-01 10:53:25 Clinical research Clinical data management Pharmaceutical industry Electronic common technical document Digital media Electronic submission Validation
67	Change of future MAH Interested Parties meeting - November 2015 Problem statement • Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-11-27 10:53:15 Clinical research Clinical data management Electronic common technical document Documentation
68	London, January, 2010 EMA Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-18 07:12:04 Clinical research Clinical data management Electronic common technical document Pharmaceutical industry Common Technical Document Pharmaceuticals policy Marketing authorization ASMF Portable Document Format
69	COD Guide to Fully Valid XML Documents Federal Student Aid fully validates all Common Record batches against the published COD Common Record XML Schema before processing them. A school can use an XML validator program to Add to Reading List Source URL: ifap.ed.gov Language: English - Date: 2014-12-10 14:07:15 Computing Markup languages Technical communication XML schema OPML Oxygen XML Editor Document type definition
70	Open Document Format Open Systems For Open Minds Dave Edstrom Technical Director Chief Technologist US-SW Practice Add to Reading List Source URL: xml.fido.gov Language: English - Date: 2006-06-26 22:27:32 Java platform Sun Microsystems Computing platforms Cross-platform software Java NetBeans Common Development and Distribution License

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