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Argus IRB Site Questionnaire: Investigator Protocol: # Is this the first submission to an IRB? Yes no If no, please explain below, and attach a letter from your local IRB, if an existing one is delegating
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How to fill out argus irb site questionnaire

01
To fill out the Argus IRB site questionnaire, follow these steps:
02
Access the Argus IRB website.
03
Login using your credentials.
04
Navigate to the 'Site Questionnaire' section.
05
Read and understand the instructions provided.
06
Fill out the questionnaire accurately and thoroughly.
07
Double-check all the entered information for any errors or omissions.
08
Save or submit the completed questionnaire as per the instructions.
09
If required, contact the Argus IRB support team for any assistance or clarification.

Who needs argus irb site questionnaire?

01
The Argus IRB site questionnaire is required by individuals or organizations involved in conducting clinical research studies. This includes principal investigators, research coordinators, study sponsors, and any other parties involved in the ethical and regulatory oversight of the study.
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Argus IRB site questionnaire is a form that collects information about the site where clinical research is being conducted.
Investigators and research sites are required to file the Argus IRB site questionnaire.
The Argus IRB site questionnaire can be filled out online or through a paper form provided by the IRB.
The purpose of the Argus IRB site questionnaire is to ensure that the research site is compliant with regulations and can provide a safe environment for research participants.
Information such as site facilities, resources, personnel qualifications, and IRB approval status must be reported on the Argus IRB site questionnaire.
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