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Clinical site
Results: 565

#	Item
191	NIAMS DSM Reports Closed_Single-site_1[removed]docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-24 15:58:55 Safety monitoring Adverse event Science Technology Business Clinical research Pharmaceutical industry Data monitoring committees
192	Single-site MOOP APPENDICES.docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 11:54:48 Pharmaceutics Science Serious adverse event Clinical trial Adverse event Methadone X Window System Function Clinical research Pharmaceutical industry Research
193	Multi-site MOOP APPENDICES_1.docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 14:28:14 Pharmaceutics Science Serious adverse event Clinical trial Adverse event Methadone X Window System Function Clinical research Pharmaceutical industry Research
194	NIAMS Data and Safety Monitoring (DSM) Report Template for Single Site Studies Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-24 15:58:26 Scientific method Science Clinical research Research Data monitoring committees
195	NIAMS DSM Reports Open_Single-site_1[removed]docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-24 15:37:26 Case report form Adverse event Safety monitoring Clinical research Pharmaceutical industry Data monitoring committees
196	NIAMS Data and Safety Monitoring (DSM) Report Template for Single-Site Studies Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-24 15:17:16 Clinical Data Management Pharmaceutics Case report form Data monitoring committees Adverse event Design of experiments Clinical trial Monitoring in clinical trials Clinical research Research Pharmaceutical industry
197	8th January 2010 To: European Commission Unit ENTR/F/2, Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:22 Pharmaceutical sciences Clinical trial Good Clinical Practice Clinical Trials Directive Ethics Committee Institutional review board Clinical site Clinical research Research Science
198	NIAMS Data and Safety Monitoring (DSM) Report Template for Multi-Site Studies Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-24 15:17:03 Clinical Data Management Case report form Data monitoring committees Adverse event Monitoring in clinical trials Clinical trial Clinical research Research Pharmaceutical industry
199	C L I N I C A L T R I A L M AGNIFIER US FDA site inspection findings during the post ICH period, [removed], fail to justify clinical research globalization concerns as recently put forth in the US and EU Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:31:22 Pharmaceutics Science Clinical trials registry Clinical trial PAREXEL Medical education Clinical research Pharmaceutical industry Research
200	TEMPLATE INSTRUCTIONS The protocol template is a tool to facilitate rapid protocol development. It is not intended to supersede the role of the Protocol Chair in the authoring and scientific development of the protocol Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2014-12-01 20:14:01 Pharmacology Health Cancer organizations Cancer Trials Support Unit Clinical trial Regulatory requirement Clinical site Clinical research Research Medicine

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