Examples of Research Site in a sentence
In addition to the Protocol all associated documents, including informational documents and advertisements, must be reviewed and approved by the appropriate IRB(s) before starting the research at each Clinical Research Site.
That in order to encourage scientific research into atmospheric processes and astronomical phenomena, and to preserve conditions nec- essary for that research, there is hereby estab- lished the Langmuir Research Site (hereinafter referred to as the ‘‘research site’’) in the Cibola National Forest in the State of New Mexico.(Pub.
If the donor is age > 18 y will be screened and evaluated by Dr. Li in the Adult Gastroenterology Clinic (see Research Site, section D.3) with a complete history and physical to ascertain eligibility.
The SOSSEC, Inc., AFRL/RIEB of the Information Directorate, Air Force Research Laboratory (AFRL), Rome Research Site (RRS) and the Naval Information Warfare Center (NIWC) Pacific (PAC) are soliciting proposals under this announcement for Common Data Link (CDL) Cognitive Radio Networking Prototype.
Langmuir Research Site; establishmentThat in order to encourage scientific research into atmospheric processes and astronomical phenomena, and to preserve conditions nec- essary for that research, there is hereby estab- lished the Langmuir Research Site (hereinafter referred to as the ‘‘research site’’) in the Cibola National Forest in the State of New Mexico.(Pub.
The Research Site shall make available to the University, and shall cause its employees and agents to make available to the University, documentation required by the Designated IRB to perform the services hereunder.
Beniston University of Geneva, Chair for Climate Research, Site de Battelle / D, 7, chemin de Drize, 1227 Geneva, Switzerland changes to a hydrological model.
The Research Site shall provide a copy of its FWA to the University, if it has an FWA.
If the Research Site has filed an FWA with the U.S. Department of Health and Human Services, Office of Human Research Protections (OHRP), it is the sole responsibility of the Research Site to identify the Designated IRB on its FWA approved by the OHRP.
If the Research Site has filed an FWA, the University agrees that the review and continuing oversight performed by the Designated IRB will meet the human subjects protection requirements of the Research Site’s FWA (the “FWA Requirements”); provided, however, that the Research Site shall not modify the FWA Requirements without the prior written consent of the University.