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Common Technical Document
Results: 587

#	Item
51	XML delivery file for all submissions via Gateway and Web Client - Statement of Intent Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:48 Clinical data management Clinical research Electronic common technical document Digital media Research Electronic submission Form Publishing Drug Master File
52	CR Acceptable Usage Policy Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:46 Clinical data management Clinical research Electronic common technical document Pharmaceuticals policy Agencies of the European Union European Medicines Agency EUDRANET Common Technical Document Application programming interface Repository
53	centercenterSupporting Document Mandatory Technical Document Add to Reading List Source URL: www.commoncriteriaportal.org Language: English - Date: 2016-07-22 07:40:10 Symmetric-key algorithm RSA Security Target Evaluation Common Criteria Advanced Encryption Standard FIPS 140-2
54	BOOKS ABOUT QUALITY TRANSMISSION 5R55N Cityhalllosangeles.com QUALITY TRANSMISSION 5R... Add to Reading List Source URL: q.cityhalllosangeles.com Language: English - Date: 2015-03-05 01:53:21 Clinical research Clinical data management Quality Quality management system Voice over IP National Accreditation Board for Hospitals & Healthcare Providers Common Technical Document
55	EU Module 1 Specification - Annex VersionNovember 2011 Document Control Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:45 Clinical data management Clinical research Electronic common technical document European Union
56	CMD(h) meeting with interested parties Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-05-29 10:17:02 Clinical research Pharmaceuticals policy Drug safety Healthcare quality Clinical data management Electronic common technical document Pharmacovigilance
57	Practical Guidance For the Paper Submission of Regulatory Information in Support of a Marketing Authorisation Application When Using an eCTD or a NeeS as the Source Submission. v2.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:51 Clinical research Clinical data management Electronic common technical document Pharmaceutical industry Pharmaceuticals policy Common Technical Document Marketing authorization Electronic submission Drug Master File
58	European Medicines Agency Evaluation of Medicines for Human Use London, August 2009 EMEA V1.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:52 Clinical research Clinical data management Pharmaceutical industry Electronic common technical document Pharmaceuticals policy Marketing authorization Probability distribution Validation
59	DOC Document Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2016-07-20 07:22:57 Clinical research Pharmaceutical industry Clinical data management Drug safety Electronic common technical document Supplementary protection certificate European Medicines Agency Summary of Product Characteristics Pharmacovigilance Validation Drug Master File
60	18 March 2015 EMAProcedure Management and Business Support Division Use of XML delivery file for submissions via eSubmission Gateway / Web Client – phased implementation for all Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:00 Clinical data management Clinical research Electronic common technical document Digital media Research Electronic submission Form European Medicines Agency

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