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#	Item
941	State v. De Frank, ____ N.J. Super. _____ (App. Div[removed]Defendant was convicted of DWI. At trial, a certificate signed by the nurse who drew a sample of his blood for alcohol content analysis was admitted into eviden Add to Reading List Source URL: www.judiciary.state.nj.us Language: English - Date: 2011-05-20 13:56:30 Notary Law Notary public
942	Attachment A. SACHRP Recommendations on Consideration of Local Context with Respect to Increasing Use of Single IRB Review SACHRP recognizes that there is increased use of single IRBs for review for multi-site studies, a Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2014-09-11 00:35:37 Scientific method Clinical trial Office for Human Research Protections Public Responsibility in Medicine and Research Institutional review board Adverse event Human subject research Clinical research coordinator Clinical research Research Science
943	ANDREA GEORGE Andrea George is the Executive Director of the Federal Defenders of the Eastern District of Washington and Idaho. From 1989 to 2011, she was an Assistant Federal Defender for the District of Minnesota and h Add to Reading List Source URL: www.waed.uscourts.gov Language: English - Date: 2014-03-21 12:17:29 Legal aid Public defender Prosecutor Gonzaga University School of Law Mock trial Criminal defense lawyer Spokane Washington Law Criminal procedure Legal professions
944	Opinions of the Colorado Supreme Court are available to the public and can be accessed through the Court’s homepage at http://www.courts.state.co.us Opinions are also posted on the Colorado Bar Association homepage at Add to Reading List Source URL: www.courts.state.co.us Language: English - Date: 2012-08-09 18:33:17 Civil procedure Work-product doctrine Trial
945	Federal Register / Vol. 66, No[removed]Tuesday, April 24, [removed]Rules and Regulations be misleading and is in need of clarification. ACTION: Interim rule; opportunity for public comment. Add to Reading List Source URL: www.fda.gov Language: English - Date: 2001-04-24 02:41:11 Research Food and Drug Administration Pharmacology Pharmaceutical industry Drug safety Institutional review board Investigational Device Exemption Clinical trial Investigational New Drug Medicine Health Clinical research
946	PATENT SETTLEMENTS ARE PRO-CONSUMER – SPEED ACCESS TO AFFORDABLE MEDICINES THE ISSUE Banning patent settlements is anti-consumer. A settlement guarantees early market entry, unlike the risk of a trial loss. As a result Add to Reading List Source URL: www.gphaonline.org Language: English - Date: 2013-03-01 19:33:30 Patent law Pharmacology Generic drug Public domain Law Generic brand Patent Evergreening Drug Price Competition and Patent Term Restoration Act Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
947	Crimes Amendment Act (No[removed]Public Act Date of assent Commencement Add to Reading List Source URL: www.legislation.govt.nz Language: English - Date: 2013-04-28 18:06:50 Juries Government English criminal law Jury trial Legal terms Acquittal Sexual Offences (Amendment) Act No case to answer Law Criminal procedure Criminal law
948	NIH – Genetic Test Registry - Request for Comments 1. Tests which include genetic technologies, but are not testing for germline or somatic genetic differences may be less relevant to include – e.g. PCR for HIV virus Add to Reading List Source URL: osp.od.nih.gov Language: English - Date: 2013-10-22 11:49:40 Medical genetics Nursing research Genomics Medical tests Medical ethics Genetic testing Public health genomics Genetic counseling Clinical trial Medicine Health Science
949	ATTORNEY FOR APPELLANT ATTORNEYS FOR APPELLEES Mark Small Marion County Public Defender Agency Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-03-26 11:53:17 Magistrate Hearing Legal procedure Law Trial
950	Guide to the Institutional Review Board (IRB) at the University of Nebraska–Lincoln Add to Reading List Source URL: research.unl.edu Language: English - Date: 2012-08-21 10:23:40 Science Institutional review board Belmont Report Office for Human Research Protections Clinical trial Public Responsibility in Medicine and Research Common Rule Human subject research Grant Clinical research Research Ethics

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