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Clinical Data Management
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211	PDF Document Add to Reading List Source URL: www.journalslibrary.nihr.ac.uk Language: English - Date: 2013-09-26 21:39:44 Clinical Data Management EudraCT Pharmaceutical industry Epidemiology Newcastle University Protocol Internet Clinical trial Clinical research Research Science
212	PDF Document Add to Reading List Source URL: www.pointcrosslifesciences.com Language: English - Date: 2014-05-12 19:05:14 Research Statistics Clinical Data Management Data warehousing Food and Drug Administration Metadata Data extraction Clinical Data Interchange Standards Consortium Hoffmann-La Roche Science Data management Clinical research
213	PDF Document Add to Reading List Source URL: www.corc.uk.net Language: English - Date: 2014-04-01 10:57:11 Patient-reported outcome Outcomes research Evaluation methods Science Evaluation Educational psychology Clinical research Epidemiology Clinical Data Management
214	PDF Document Add to Reading List Source URL: www.ispor.org Language: English - Date: 2015-04-28 16:04:01 Clinical research Science Epidemiology Clinical Data Management Health informatics Pharmacoeconomics Comparative effectiveness research Outcomes research Health technology assessment Health Medicine Health economics
215	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Clinical research Clinical Data Management Drug safety Medical informatics Electronic Common Technical Document Investigational New Drug Common Technical Document New Drug Application Office of Regulatory Affairs Medicine Research Food and Drug Administration
216	PDF Document Add to Reading List Source URL: www.niaid.nih.gov Language: English - Date: 2015-03-17 10:34:43 Case report form Protocol Quality assurance Informed consent Behavior Ethology Science Clinical Data Management clinical research Medical ethics
217	Procedure for Development of the GMP+ FC scheme 1 Introduction A standard (or requirements and conditions of a standard) of the GMP+ FC scheme is developed during a number of stages in close cooperation and consultation Add to Reading List Source URL: www.gmpplus.org Language: English Quality Validation Validity SQL Data management Notation Pharmaceutical industry Computing Clinical research
218	Requirements on Submissions for Periodic safety update reports (PSUR) to National Competent Authorities (NCAs) for products authorised via National Procedures, MRP and DCP (NAPs) Doc. Ref.: CMDh, Rev.1 September Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-03-10 10:40:36 Clinical Data Management Clinical research Electronic Common Technical Document
219	Sixth International Workshop on Comparative Survey Design and Implementation Ann Arbor, Michigan – United States, 5-7 March, 2009 Towards the development of a checklist to control Add to Reading List Source URL: www.csdiworkshop.org Language: English - Date: 2013-01-12 16:08:08 Clinical Data Management Patient-reported outcome Messaging Application Programming Interface Science Validation Technology Knowledge Clinical research Translation Linguistic validation
220	Training: eCTDmanager Refresher Training – One Day Duration Two days (ca. 09:00-17:00h) Agenda Timetable Add to Reading List Source URL: www.extedo.com Language: English - Date: 2012-10-31 04:50:41 Electronic Common Technical Document International Space Station CoFFEE Spaceflight Clinical Data Management Clinical research