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Este formulario se utiliza para presentar un estudio clínico iniciado por un investigador a Oxford Immunotec para consideración de apoyo, que incluye detalles sobre el título del estudio, hipótesis, objetivos, diseño del estudio y presupuesto.
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How to fill out investigator initiated study proposal

01
Begin with a clear title for the study proposal.
02
Introduce the background and rationale for the study.
03
Define the study objectives and hypothesis.
04
Describe the study design and methodology.
05
Outline the participant recruitment process.
06
Detail the data collection methods and instruments.
07
Discuss the statistical analysis plan.
08
Address potential ethical considerations and approvals needed.
09
Provide a timeline for the study.
10
Include a budget and funding sources if applicable.
11
List references and relevant literature.

Who needs investigator initiated study proposal?

01
Researchers looking to conduct clinical trials.
02
Healthcare professionals intending to explore new treatment methods.
03
Institutions seeking to investigate specific health-related questions.
04
Pharmaceutical companies interested in innovative study designs.
05
Funding organizations assessing study proposals for grant approvals.
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An investigator initiated study proposal is a research plan created by an investigator, rather than a pharmaceutical company or other sponsor, aiming to explore a specific hypothesis or research question.
Investigators, typically researchers or clinicians with the necessary credentials and expertise, are required to file investigator initiated study proposals.
To fill out an investigator initiated study proposal, the investigator should provide detailed information about the study's objectives, methodology, design, funding, and compliance with ethical guidelines.
The purpose of an investigator initiated study proposal is to outline a planned research study that seeks to answer key scientific questions, assess new treatments or interventions, and advance medical knowledge.
Information that must be reported includes study objectives, hypothesis, study design, participant criteria, data collection methods, statistical analysis plans, and any potential risks and benefits.
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