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Multimeter Supplement Date: IR File#: Protocol #: Principal Investigator: Study Title: SECTION A Performance Sites where Fred Hutch is the IRB of Record:1. Are there performance sites outside the
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How to fill out multi-center supplement

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Start by gathering all the necessary information and documents related to the multi-center supplement form.
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Read the instructions provided with the form to understand the requirements and any specific guidelines.
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Begin filling out the form by providing your personal details such as name, address, contact information, etc.
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Follow the designated sections in the form to input information about each center you are adding to the supplement.
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Who needs multi-center supplement?

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The multi-center supplement is typically needed by organizations or individuals operating multiple centers or facilities. This could include businesses with multiple branch locations, educational institutions with multiple campuses, healthcare providers with multiple clinics or hospitals, and so on. The supplement allows for central coordination and compliance reporting by listing all the centers under a single entity.

What is Multi-Center Supplement Form?

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Multi-center supplement is a document used to report additional information or updates related to a clinical trial that involves multiple study locations.
The sponsor or principal investigator of a clinical trial is typically required to file a multi-center supplement.
To fill out a multi-center supplement, the sponsor or principal investigator must provide the requested information such as study location updates, protocol modifications, adverse event reports, etc.
The purpose of a multi-center supplement is to ensure transparency and accuracy in reporting information related to clinical trials conducted at multiple study locations.
Information that must be reported on a multi-center supplement includes protocol modifications, adverse events, study location updates, and any other relevant updates.
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