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Clinical data management
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81	Republic of the Philippines DEPARTMENT OF LABOR AND EMPLOYMENT Intramuros, Manila Office Performance Commitment and review (OPCr) Add to Reading List Source URL: dole.gov.ph Language: English - Date: 2014-01-14 02:18:22 Clinical data management Clinical research Pharmaceutical industry Quality Validation Validity
82	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
83	TAG Inventory Quality Guidelines version 2.1 Summary of Revisions The Trustworthy Accountability Group (TAG) Inventory Quality Guidelines (IQG) promote the flow of advertising budgets into digital advertising with indust Add to Reading List Source URL: tagtoday.net Language: English - Date: 2015-12-17 15:04:07 Pharmaceutical industry Validity Clinical data management Clinical research Quality Validation Advertising Professional certification
84	Copernicus Land Monitoring Services Validation of CORINE Land Cover Products Summary of preliminary results 1. Context This document aims at covering the validation of CORINE Land Cover (CLC) data set, specifically the C Add to Reading List Source URL: land.copernicus.eu Language: English - Date: 2015-12-18 04:50:17 Pharmaceutical industry Validity Clinical data management Clinical research Quality Validation Coordination of Information on the Environment
85	Annex 2 to the HMA eSubmission Roadmap: Implementation of mandatory eCTD format for regulatory submissions (Status: Final version adopted by the eSubmission CMB. Dated 26 JulyScope This annex is intended for both Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:41 Clinical research Clinical data management Electronic common technical document Pharmaceutical industry Pharmaceuticals policy Marketing authorization Electronic submission
86	23 June 2016 EMAversion 1.1 Periodic Safety Update Report (PSUR) repository mandatory use: questions and answers Information for Marketing Authorisation Holders on how to submit a PSUR 1. What is the PSUR r Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:04 Clinical research Clinical data management Electronic common technical document Agencies of the European Union Pharmaceuticals policy
87	Updated 08 JulyRelease Notes Detailing the updates of the EU eCTD Module 1 Specification The published version 3.0 has been updated to versionto correct pick list values and the updated version was publishe Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:41 Clinical data management Clinical research Identifiers Universal identifiers Pharmaceutical industry Universally unique identifier Electronic common technical document Validation Globally unique identifier
88	 HOME STUDY The Evolving World of Metrics Are Performance Metrics About Doing the Right Things or Simply Doing Things Right? Add to Reading List Source URL: www.acrpnet.org Language: English - Date: 2016-07-29 11:46:01 Clinical research Pharmaceutical industry Drug discovery Process management Healthcare quality Clinical trial Performance metric Business process improvement Drug development Medical guideline Risk management Clinical Data Inc
89	E-submission-GL- VerSeptember 15 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:07 Clinical data management Clinical research Electronic common technical document Pharmaceutical industry Digital media Directory structure Common Technical Document Folder Computer file Marketing authorization Directory Electronic submission
90	Implementation guide for EU eCTD M1 specification Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:42 Clinical data management Clinical research Quality Identifiers Universal identifiers Electronic common technical document Validation Universally unique identifier Globally unique identifier Specification

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