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TOOL 1.6 Site Feasibility AssessmentINSTITUTIONAL LOGOS ite Feasibility Assessment Site namesake type (e.g. hospital, clinic)Place / health zoneCountry (province / district)Date of assessmentDepartment
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01
Understand the purpose of the protocol feasibility.
02
Clearly define the study objectives and endpoints.
03
Identify and engage key stakeholders early in the process.
04
Gather relevant data and information to support the feasibility assessment.
05
Analyze the potential risks and challenges that may impact the study.
06
Develop a detailed plan with timelines and milestones for protocol feasibility improvement.
07
Review and revise the protocol feasibility document as needed to address any identified gaps or issues.

Who needs protocol feasibility to improve?

01
Clinical researchers and study sponsors who want to ensure the success and efficiency of their clinical trials.
02
Regulatory agencies and ethics committees looking to approve studies with well-constructed feasibility assessments.
03
Healthcare providers involved in the design and implementation of clinical research protocols.
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Protocol feasibility to improve refers to the assessment of whether a proposed protocol can be successfully implemented and achieve the desired outcomes.
The individuals or team responsible for the development and implementation of the protocol are required to file protocol feasibility to improve.
Protocol feasibility to improve can be filled out by providing detailed information on the proposed protocol, including objectives, methodology, resources needed, and potential challenges.
The purpose of protocol feasibility to improve is to ensure that the proposed protocol is realistic, achievable, and will lead to the desired outcomes.
Information that must be reported on protocol feasibility to improve includes objectives, methodology, resources needed, potential challenges, timeline, and expected outcomes.
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