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The PHS Human Subjects and Clinical Trials Information form is used to collect information on human subjects research, clinical research, and/or clinical trials, including study population characteristics, protection and monitoring plans, and a protocol synopsis.
Assignment Request means a request by a Seller, in a form specified by Magellan, to assign all or part of storage capacity from previous storage rights held in the form of a Long Term Storage Agreement to Magellan for delivery to a Buyer in the form of a CAC. \u201c
1.1 Abbreviations AbbreviationFull Meaning of AbbreviationNICHDEunice Kennedy Shriver National Institute for Child Health and Human DevelopmentNIDCRNational Institute of Dental and Craniofacial ResearchNIGMSNational Institute of General Medical SciencesNIHNational Institutes of Health181 more rows
The PHS Assignment Request Form may be used to communicate specific application assignment and review requests to the Division of Receipt and Referral (DRR) and to Scientific Review Officers (SROs).
NIH encourages you to submit an Assignment Request Form with your application. The form allows you to: Express a preference for a particular scientific review group (or \u201cstudy section\u201d) Express a preference for a specific awarding component (an NIH Institute or Center)
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National Institutes of Health The largest of the PHS agencies, NIH is organized into 13 research institutes, primarily by disease or population categories (cancer, heart disease, aging, etc.), plus the National Library of Medicine and seven research and support divisions (Figure 1-4 ).
3. Is proprietary/privileged information included in the application? This field is required. Patentable ideas; trade secrets; or privileged, confidential commercial, or financial information should be included in applications only when such information is necessary to convey an understanding of the proposed project.
Private identifiable specimens, records and data about individuals are considered to be human subjects, even if the researcher has no contact or interaction with the individuals. \u201cThird party\u201d or \u201csecondary\u201d subjects.
Clinical trials are research studies performed in people that are aimed at evaluating a medical, surgical, or behavioral intervention. They are the primary way that researchers find out if a new treatment, like a new drug or diet or medical device (for example, a pacemaker) is safe and effective in people.
The PHS Human Subjects and Clinical Trials Information Form is used to collect information on: human subjects research. clinical research and/or clinical trials. study population characteristics. protection and monitoring plans.

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