Even then, Caltrans wouldn't be free to sell the homes until the Federal Highway Administration accepted the proposed route for a tunnel or whatever project was approved and the state determined which properties were "excess" and therefore available to be sold, said Kelly Markham, a Caltrans spokeswoman.
Similarly, after listening to 1,159 testimonies against the Enbridge Northern Gateway and only two for it, they approved the project and determined that "Canada and Canadians would be better off with the Enbridge Northern Gateway project than without it".
On the basis of Ethical Guidelines for Medical and Research Involving Human Subjects in Japan, the Institutional Review Board of The University of Tokyo approved this research and determined that individual informed consent was not required (No. 10421).
The Charles R. Drew University institutional review board approved the study and determined that an informed consent was not necessary for individuals screened with a point-of-care A1C test because screening for diabetes often takes place at community sites, including health fairs, churches, and senior citizen centers.
This study was Institutional Animal Care and Use Committee (IACUC) approved and designed to determine whether this diet is better tolerated and equally effective to acidification with citric acid against gut colonization and subsequent bacterial translocation in a premature infant rabbit model.
Federal law and University policy require that all research you conduct that involves human subjects in any way must be reviewed and approved or determined to be exempt by the CPHS before the research is initiated.
This study was approved by the Johns Hopkins Bloomberg School of Public Health Institutional Review Board and determined to be exempt.
Cleveland Clinic institutional board review approved the study protocol and determined that it meets criteria for waiver for consent.
Western Institutional Review Board® (Olympia, WA) approved the study protocol and determined that the study met requirements for waiver of consent and waiver of authorization for use and disclosure of protected health information on August 24 , 2012
This project was approved by the Center for Disease Control and Prevention Institutional Review Board IRBB) and determined to be public health surveillance (rather than human subjects research), and therefore not requiring institutional review board review, by the California Committee for the Protection of Human Subjects.
With the abundance of newer agents recently approved and in the research pipeline, determining the most cost-effective strategy through empirical research will be the primary goal for all stakeholders, including patients.
