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APPLICATION FORM FOR RESIDENT RESEARCH GRANTA. COVER PAGE GRANT APPLICATION (to be completed by the investigator(s))1. Title of Proposal:2. Investigators: Diplomate Supervisor: Name, degree TitleSignatureMailing
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How to fill out 1 investigator-initiated study research

01
Determine the research question or objective of the investigator-initiated study.
02
Develop a study protocol that outlines the study design, inclusion criteria, exclusion criteria, and any interventions or procedures.
03
Obtain necessary approvals from the appropriate Institutional Review Board (IRB) or Ethics Committee.
04
Recruit participants who meet the inclusion criteria for the study.
05
Obtain informed consent from all participants before their involvement in the study.
06
Collect data according to the study protocol, using appropriate research instruments and methods.
07
Analyze the collected data using appropriate statistical methods or qualitative analysis techniques.
08
Interpret the results of the study and draw conclusions based on the findings.
09
Prepare a research report or manuscript that includes an introduction, methods, results, discussion, and conclusion sections.
10
Submit the research report or manuscript to a peer-reviewed journal for publication.
11
Present the findings of the investigator-initiated study at conferences or scientific meetings, if desired.

Who needs 1 investigator-initiated study research?

01
Researchers or scientists who have a specific research question and wish to investigate it in a systematic manner.
02
Academic institutions or research organizations that encourage and support independent research initiatives.
03
Healthcare professionals who want to explore alternative treatments or interventions for a specific condition.
04
Funding agencies or grant providers who require evidence-based research to fund new projects or interventions.
05
Government agencies or regulatory bodies that need scientific evidence to inform policies or regulations.
06
Pharmaceutical companies or medical device manufacturers who want to conduct non-sponsored research to evaluate the safety and efficacy of their products.
07
Individuals or patient advocacy groups who are interested in generating new knowledge and advancing medical science.

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An investigator-initiated study research is a research project that is initiated and conducted by a researcher rather than a pharmaceutical company or other sponsor. The investigator designs the study, collects data, and analyzes the results, typically to investigate a specific hypothesis or research question.
Researchers or investigators who are conducting studies that they have initiated are required to file for investigator-initiated study research. This may include academic researchers, clinical investigators, or other professionals engaged in research.
Filling out an investigator-initiated study research typically involves completing application forms provided by the relevant regulatory or institutional review boards. Researchers must include detailed information about the study's objectives, methodology, participant recruitment, data analysis plans, and ethical considerations.
The purpose of investigator-initiated study research is to advance scientific knowledge, test new treatments or interventions, and address specific research questions or hypotheses that may not be driven by commercial interests.
Information that must be reported includes the study's objectives, participant demographics, methodology, results, adverse events, and conclusions drawn from the research. Additionally, compliance with ethical standards and regulatory requirements should be documented.
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