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Drug design
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991	Name [please print]: ______________________________________ NCIC CTG Centre Code: Add to Reading List Source URL: www.ctg.queensu.ca Language: English - Date: 2014-07-08 08:30:39 Law Science Design of experiments Clinical trial Drug discovery Pharmaceutical industry National Crime Information Center Royalties Conflict of interest Pharmacology Clinical research Research
992	Microsoft Word[removed]en.doc Add to Reading List Source URL: www.admin.ch Language: English - Date: 2014-11-24 17:40:28 Science Pharmacology Scientific method Design of experiments Drug safety Clinical trial Institutional review board Good Clinical Practice Clinical research coordinator Clinical research Research Pharmaceutical industry
993	University Of Maine at Farmington Institutional Review Board (IRB) Application for Review of Research Add to Reading List Source URL: www2.umf.maine.edu Language: English - Date: 2014-06-05 15:57:11 Science Medical ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Psychology Human subject research Clinical research Research Ethics
994	INSTRUCTIONS FOR REQUESTING AN EXEMPTION FROM FULL IRB REVIEW Add to Reading List Source URL: www2.umf.maine.edu Language: English - Date: 2014-06-05 15:57:10 Design of experiments Pharmacology Scientific method Medicine Pharmaceutical industry Institutional review board Clinical research coordinator Clinical research Research Drug safety
995	University Of Maine at Farmington Add to Reading List Source URL: www2.umf.maine.edu Language: English - Date: 2014-06-05 15:57:09 Science Medical ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Psychology Human subject research Clinical research Research Ethics
996	Microsoft Word[removed]en.doc Add to Reading List Source URL: www.admin.ch Language: English - Date: 2015-01-17 15:44:52 Science Design of experiments Drug safety Institutional review board Pharmacology Dignity Ethics Autonomy Behavior
997	Verification of Research Subject or Participant Compliance (To be filed with dissertation proposals, final dissertations, final theses, and final capstones) Student Name: ______________________________________ Last 4 num Add to Reading List Source URL: www.unco.edu Language: English - Date: 2015-01-13 11:41:42 Ethics Animal testing Design of experiments Pharmacology Drug safety Institutional Animal Care and Use Committee Institutional review board Thesis Compliance Knowledge Clinical research Education
998	FDA Decisions for Investigational Device Exemption Clinical Investigations - Guidance for Sponsors, Clinical Investigators, Institutional Review Boards, and Food and Drug Administration Staff Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmaceutical industry Pharmacology Design of experiments Food and Drug Administration Investigational Device Exemption Clinical trial Institutional review board Medical device Clinical research Research Medicine
999	[removed]Saint Leo University Institutional Review Board – Application for IRB Review of Proposed Research All Word processor files should be combined into ONE file for submission, with supplemental files placed Add to Reading List Source URL: www.saintleo.edu Language: English - Date: 2013-12-16 13:25:30 Design of experiments Pharmacology Behavior Drug safety Research Institutional review board Email Psychology Informed consent Clinical research Medical ethics Science
1000	APPLICATION INSTRUCTIONS Letter of Intent (LOI) Instructions To begin the application process, click the link below: http://www.alzdiscovery.org/research-and-grants/applyforfunding Click on the Academic or Biotech tab on Add to Reading List Source URL: www.alzdiscovery.org Language: English - Date: 2015-01-20 13:00:56 Research Pharmaceutical sciences Pharmaceutics Food and Drug Administration Design of experiments Clinical trial Pre-clinical development Pharmaceutical industry Drug discovery Clinical research