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Health Care Personnel Education and Credentialing Section2709 Mail Service Center Raleigh, NC 276992709 Division of Health Service RegulationPhone: 9198553970 Fax: 9197339764 N.C. Department of Health
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Obtain the necessary forms for the clinical site addition from the appropriate office or department.
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Fill out the forms completely and accurately, providing all the required information about the new clinical site.
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Submit the completed forms to the designated individual or department for review and approval.
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Follow up on the progress of the site addition request and make any necessary revisions or updates as requested.
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Once the request is approved, ensure that all necessary parties are notified and updated on the new clinical site.

Who needs clinical site addition for?

01
Individuals or organizations who are looking to add a new clinical site to an existing program or network.
02
Healthcare providers, researchers, or educators who need to expand their reach or resources by establishing a new clinical site.
03
Students or trainees who require access to a specific clinical site for educational or training purposes.
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Clinical site addition is for adding new locations where clinical trials or medical research studies will take place.
Sponsors or principal investigators overseeing the clinical trials are required to file clinical site addition.
You can fill out the clinical site addition form by providing details of the new site, contact information, and any relevant protocols.
The purpose of clinical site addition is to expand the locations where clinical trials can be conducted.
Information such as site name, address, principal investigator, IRB approval status, and study protocols must be reported on clinical site addition.
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