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Clinical trial protocol
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21	The role, duties and responsibilities of clinical trials personnel Monitoring: rules and recommendations Maria Luisa Paoloni OPBG Clinical & Research Services Add to Reading List Source URL: www.unicri.it Language: English - Date: 2012-08-07 10:48:20 Science Pharmaceutical sciences Design of experiments Pharmacology Clinical trial Institutional review board Good Clinical Practice Regulatory requirement Protocol Clinical research Research Pharmaceutical industry
22	COMMITTEE ON HUMAN RESEARCH Add to Reading List Source URL: www.research.ucsf.edu Language: English - Date: 2015-05-08 15:32:46 Science Health Design of experiments Pharmacology Food and Drug Administration Clinical trial Health Insurance Portability and Accountability Act Transmission Control Protocol Clinical research Pharmaceutical industry Research
23	Protocol Number: EudraCT Number: REC Ref: ISRCTN Ref: EME Add to Reading List Source URL: ushamp-build.squiz.co.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
24	Interlaken Leadership Awards Protocol Template Add to Reading List Source URL: www.interlakenleadershipawards.com Language: English - Date: 2015-02-15 19:44:58 Design of experiments Clinical research Pharmacology Evaluation methods Medical statistics Clinical trial Placebo Clinical study design Analysis of variance Science Statistics Information
25	Trials BioMed Central Study protocol Add to Reading List Source URL: www.trialsjournal.com Language: English Knowledge Design of experiments Epidemiology Evaluation methods Medical statistics Randomized controlled trial Meta-analysis Clinical trial Evidence-based medicine Science Research Clinical research
26	GENERAL ASPECTS AND PRINCIPLES OF ICHGCP (GOOD CLINICAL PRACTICE) Umberto Filibeck Former Head of AIFA GCP Inspectorate and GCP Promotion Unit UNICRI Consultant for Projects on GCP of CTs in developing countries Add to Reading List Source URL: www.unicri.it Language: English - Date: 2012-08-07 10:48:19 Scientific method Institutional review board Good Clinical Practice Clinical trial Clinical site Declaration of Helsinki Ethics Committee Regulatory requirement Protocol Clinical research Research Science
27	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
28	ANNEX 1 AF Contents of a Submitted Package Protocol Number:……………….. Initial Review Submitted Package Protocol Summary Sheet or Memorandum Application Form for Initial R Add to Reading List Source URL: www.health.gov.bt Language: English - Date: 2014-11-24 01:41:35 Pharmaceutical industry Design of experiments Pharmacology Medical ethics Clinical trial Case report form Informed consent Protocol Clinical research coordinator Clinical research Research Science
29	Tamminga et al. BMC Cancer 2010, 10:345 http://www.biomedcentral.com STUDY PROTOCOL Open Access Add to Reading List Source URL: www.verbeteronderzoek.nl Language: English - Date: 2012-07-09 06:23:21 Clinical research Design of experiments Epidemiology Randomized controlled trial Breast cancer Intervention Psycho-oncology Cancer survivor Comorbidity Medicine Health Oncology
30	ANNEX 2 AFDocument Receipt Form Protocol Number: Submitted date: Add to Reading List Source URL: www.health.gov.bt Language: English - Date: 2014-11-24 01:41:35 Pharmaceutical industry Clinical Data Management Medical ethics Case report form Clinical trial Informed consent Email Protocol Consent Clinical research Research Science

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