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This form is designed for Physical Therapist (PT) and Physical Therapist Assistant (PTA) academic programs to collect information from clinical education sites to facilitate student placements and
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How to fill out clinical site information form
How to fill out Clinical Site Information Form (CSIF)
01
Gather necessary information about the clinical site, including name, address, and contact details.
02
Identify the principal investigator and their credentials.
03
Include details about the site’s facilities and equipment relevant to the study.
04
Specify any ethical approvals or institutional review board (IRB) approvals obtained.
05
Provide information on the anticipated patient population and enrollment capacity.
06
Fill out sections related to financial disclosures and any conflicts of interest.
07
Review all entries for accuracy and completeness before submission.
Who needs Clinical Site Information Form (CSIF)?
01
Clinical research coordinators who manage clinical trials.
02
Investigators conducting research at clinical sites.
03
Regulatory bodies assessing compliance and site suitability.
04
Sponsors looking to evaluate potential clinical trial sites.
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What is Clinical Site Information Form (CSIF)?
The Clinical Site Information Form (CSIF) is a document used to collect essential details about clinical research sites participating in clinical trials.
Who is required to file Clinical Site Information Form (CSIF)?
Clinical research sites, including hospitals, clinics, and research institutions that participate in clinical trials, are required to file the CSIF.
How to fill out Clinical Site Information Form (CSIF)?
To fill out the CSIF, sites must provide accurate and current information regarding their facilities, staff, and resources that support the conduct of clinical trials.
What is the purpose of Clinical Site Information Form (CSIF)?
The purpose of the CSIF is to ensure that all necessary information regarding a clinical research site is disclosed, which aids in the selection and evaluation of sites for conducting clinical trials.
What information must be reported on Clinical Site Information Form (CSIF)?
The information reported on the CSIF typically includes site name, location, contact details, participating investigators, facility capabilities, and any relevant certifications or accreditations.
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