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Drug Master File
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#	Item
1	Reset Form APPLICATION FOR PLAN REVIEW State FormR2Indiana State Department of Health Food Protection Program Add to Reading List Source URL: www.duboiscountyin.org Language: English - Date: 2014-02-11 13:13:30 Civil engineering Construction (Design and Management) Regulations Drug Master File
2	Release Notes for Harmonised Technical Guidance for eCTD Submissions in the EU v3.0 This document highlights the changes incorporated in version 3.0, in comparison with version 2.0, of the eCTD guidance document. For cle Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:10 Medical research Clinical research Health Clinical data management Computing Electronic common technical document Pharmaceutical industry Pharmaceuticals policy Marketing authorization Section Diff utility Drug Master File
3	EU Module 1 Specification - Annex VersionRelease Notes November 2011 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:45 Medical research Health Pharmaceutical industry Clinical data management Clinical research Electronic common technical document Pharmaceuticals policy Marketing authorization Drug Master File
4	MARYLAND DEPARTMENT OF THE ENVIRONMENT APPLICATION FOR TEMPORARY ELECTRONIC REPORTING WAIVER FACILITY INFORMATION Facility Name Facility Address Add to Reading List Source URL: www.mde.state.md.us Language: English - Date: 2016-08-18 22:22:41 ZIP Code Drug Master File
5	TECHNICAL OPERATIONS MANUAL FOR ELECTRONIC FILING IN MONTANA STATE COURTS State of Montana Judicial Branch Add to Reading List Source URL: courts.mt.gov Language: English - Date: 2016-04-20 15:53:31 Legal documents Law Judicial branch of the United States government Legal procedure Notice of electronic filing Filing Electronic Filing System Service of process Electronic court filing Drug Master File
6	CMDh_340_2015_Rev0_2015 10 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-01-07 05:29:42 Software Pharmaceutical industry Pharmaceuticals policy System software Computer architecture Drug Master File Food safety Qualified person QP Good manufacturing practice
7	DOC Document Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-06-15 05:38:43 Pharmaceutical industry Medical research Marketing authorization Business Economy Validation Email address Subroutine Drug Master File
8	Sample due diligence letter Notification letters must be sent for all property over $100, safe deposit boxes and securities. Letters must be sent no more than 120 days or less than 60 days before the report is filed. Fo Add to Reading List Source URL: www.kansascash.com Language: English - Date: 2015-11-10 11:50:56 Lost mislaid and abandoned property Personal property law Squatting Due diligence Cheque Drug Master File
9	Q&A for EMA Gateway Web Client Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:47 Clinical data management Clinical research Electronic common technical document Digital media Research Form Email Web page Electronic submission Drug Master File
10	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

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