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[DOCX File]Guideline: Study Start-up to SIV and Site Activation
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The scientific question being investigated should be described in detail. ... Begin with a section titled Experimental Design describing the objectives and design of the study as well as prespecified components. ... following order: materials and methods, figures, tables, and other files (such as movies, data, interactive images, or database ...
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DSMB Report Template
Discuss study closeout requirements and study-specific issues with DCP Medical Monitor, Scientific Monitor, and Nurse Consultant prior to initiating study closeout activities. ... analyses and upload results to database of record or other data storage system. YesNoN/A.
scientific literature database

[DOC File]Science Manuscript Template
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Most scientific research is hypothesis-driven. That is, it seeks to address a specific, measurable, and answerable question, which may be intermediate to its ultimate objective, but essential to attaining the same. ... This work may include model development, plant breeding, database development, high throughput genomics, service work, and ...
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[DOCX File]Checklist For Study Close-Out - Division of Cancer Prevention
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Changes to CRFs: After the study CRFs are approved and the study database developed, the Lead Organization should judiciously assess the impact of planned CRF modifications and submit changes only if necessary to support the scientific intent of the study. Any such changes must be submitted to NCI/DCP for review and approval along with the ...
research study database

[DOCX File]Guidelines for Developing a Single-Site, Manual of ...
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{The scientific integrity of the study and the credibility of the data from the study depend substantially on the study design. Include a brief paragraph or bulleted text describing the study design. ... “Recording” refers to documenting data in the study database. Recording events is critical for assessing. whether an event must be reported.
case study database

[DOCX File]NIDCR Clinical Study Observational Protocol
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Collect the data using instruments prepared for the study and use the information from the study database to fill out the Inclusion Enrollment Report. Study participants who self-identify with more than one race should be reported in the aggregate in the "More Than One Race" category. When reporting these data to NIH, include the following items:
clinical study database

[DOC File]National Cancer Institute (NCI)/Division of Cancer ...
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Study data must be initially captured using one or more of the following methods: on paper source documents, in electronic medical records or other electronic databases (e.g., central laboratory database), and/or in Electronic Data Capture (EDC) systems.
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[DOC File]Hypothesis and Non Hypothesis Research
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This person may collect or review data before it is entered in the study database. Data and Safety Monitoring Board (DSMB) – ... The study protocol, presented as an appendix, provides a scientific rationale of the proposed investigation. In this section of the MOP a brief overview (approximately 500-750 words) of the study protocol should be ...
scientific article database

[DOC File]Non-Competing Grant Progress Report (PHS 2590)
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Research Proposal Form. American. Heart. Association. Quality. Improvement. Programs Registry. Questions? Or Email this Form – QualityResearch@Heart.org. Date Submitted to AHA: . Project # (assigned by AHA Staff): Working Title of Research Proposal:. National Level Program Primary Database - P lease select one: Click
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The best academic research databases [2019 update] - Paperpile
This report reflects data from the study database as of April 19, 2015. Within the body of the report are summary tables of enrollment, demographic characteristics, and adverse events. Additional tables, listings, and figures referenced in this report are provided in Appendices A-C.
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Scientific study database