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Clinical trial
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#	Item
231	p-medicine_270089_D2-4 _requirements_for_VPH_v4_1 Add to Reading List Source URL: p-medicine.eu Language: English - Date: 2013-02-13 06:22:26 Physiology Health Medicine Biology Health informatics Pathology Virtual Physiological Human Medical technology VPH Bioinformatics Living Human Project Clinical trial
232	MEDICAL INNOVATION BILL 1. Introduction The questions the Academy asked itself in considering the Bill were:  Do we support the purpose and intention of the Bill?  Are we persuaded that the Bill will achieve its st Add to Reading List Source URL: www.rcoa.ac.uk Language: English - Date: 2015-03-26 11:53:45 Medical research Health Clinical pharmacology Law in the United Kingdom Medical Innovation Bill Medical law Clinical trial National Health Service Patient safety
233	Principles for Responsible Clinical Trial Data Sharing Our Commitment to Patients and Researchers Biopharmaceutical companies are committed to enhancing public health through responsible sharing of clinical trial data in Add to Reading List Source URL: www.phrma.org Language: English - Date: 2015-07-17 17:00:38 Medical research Health Pharmaceutical industry Research Clinical research Clinical trials Drug discovery Medical statistics Patient recruitment Outline of clinical research YODA Project
234	CE Objectives and Evaluation Form appear on page 99. Complimentary CE provided as an educational service by C-Change (www.cchangetogether.org). The Basics of Human Subjects Protection Linda H. Yoder Add to Reading List Source URL: c-changetogether.org Language: English - Date: 2010-11-15 14:09:03 Medical research Research Medical ethics Clinical research ethics Applied ethics Clinical research Research ethics Design of experiments Institutional review board Clinical trial Public Responsibility in Medicine and Research Human subject research
235	p-medicine – Grant Agreement noD2.1 – State of the art review of the p-medicine environment Deliverable No. 2.1 State of the art review of the p-medicine environment Add to Reading List Source URL: p-medicine.eu Language: English - Date: 2013-02-13 06:22:25 Medical research Clinical research Clinical data management Clinical trial management system Clinical trial Clinical data management system Health informatics Clinical Academic clinical trial Electronic data capture Trial master file Good clinical practice
236	p-medicine – Grant Agreement noD13.2 – CDS scenarios and requirements for the clinical decision support tool Deliverable No. D13.3 Selection and annotation of the CDS training and evaluation datasets Add to Reading List Source URL: p-medicine.eu Language: English - Date: 2013-08-09 04:21:04 Health Medical research Clinical research Health informatics Clinical trial Design of experiments Pharmaceutical industry Product testing Evidence-based medicine International Society of Paediatric Oncology Clinical decision support system Oncology
237	Running head: TIPS ON WRITING NRSA PROPOSALS 1 Tips on Writing National Research Service Award Predoctoral Fellowship Proposals From Real NRSA Reviewers Add to Reading List Source URL: www.pitt.edu Language: English - Date: 2011-01-06 14:19:54 Economy Business Medical research Clinical research Pharmaceutical industry National Research Service Award Postdoctoral research Grant writing Grantsmanship Proposal Grant Clinical trial
238	FOR IMMEDIATE RELEASE Capsugel to Acquire Xcelience and Powdersize Xcelience provides the company with specialized clinical trial manufacturing and supply capabilities for a broad range of solid dosage forms Powdersize Add to Reading List Source URL: www.xcelience.com Language: English - Date: 2015-12-14 09:27:56 Pharmacology Pharmaceutical sciences Pharmaceutical industry Dosage forms Capsugel Pfizer Pharmacokinetics Contract manufacturing organization Pharmacy
239	DOC Document Add to Reading List Source URL: people.westminstercollege.edu Language: English - Date: 2009-10-15 14:47:10 Medical research Research Applied ethics Medical ethics Clinical research Design of experiments Pharmaceutical industry Institutional review board Public Responsibility in Medicine and Research Clinical trial Human subject research Informed consent
240	Understanding the European GMO legislation for gene therapy products in clinical trials Jacqueline Barry Director of Regulatory Affairs Add to Reading List Source URL: ct.catapult.org.uk Language: English - Date: 2016-04-19 09:57:25 Biology Molecular biology Biotechnology Medical research Emerging technologies Pharmaceutical industry Bioethics Gene therapy Genetically modified organism Clinical trial Genetic engineering

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