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Department of Revenue Services Compliance Support Unit 25 Sigourney Street, Ste. 2 Hartford CT 06106-5032 (New 10/01/2011) Form AU-960 Nonresident Contractor Request for Verified Contractor Status
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How to fill out form au-960 - ctgov:

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Start by obtaining a copy of form au-960 - ctgov. This form is commonly used by individuals or organizations seeking to submit an application or proposal to the Clinical Trials.gov database.
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Carefully read the form instructions and familiarize yourself with the requirements and guidelines. It is essential to understand the purpose of the form and how to accurately complete it.
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Begin by providing your personal or organization's information in the designated sections of the form. This may include your name, contact details, and any relevant affiliations.
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Next, clearly state the title or purpose of your proposed application or trial. Make sure to use concise and descriptive language to accurately convey the nature of the study.
05
Provide a detailed summary or abstract of your proposed trial. This section should include information about the study's objectives, methodology, participant eligibility criteria, and expected outcomes.
06
If applicable, indicate any relevant funding sources for your trial. This includes information about grants, sponsorships, or any financial support that would contribute to the successful execution of your study.
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In the subsequent sections of the form, provide additional detailed information about the trial, such as the study design, intervention or treatment plan, data collection procedures, and any safeguards to ensure participant safety.
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Include any necessary attachments or supporting documents, such as study protocols, consent forms, Institutional Review Board (IRB) approvals, or other relevant certifications. It is crucial to ensure that all supporting documentation is accurately labeled and attached to the form.
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Double-check all the information you have provided, ensuring that it is accurate, complete, and well-organized. Any discrepancies or omissions could delay the processing of your application.

Who needs form au-960 - ctgov:

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Researchers or principal investigators planning to conduct clinical trials or studies and intending to register their trials with Clinical Trials.gov may need to fill out form au-960 - ctgov.
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Pharmaceutical companies or organizations developing new drugs, therapies, or medical interventions may also require this form to submit detailed information about their clinical trials for evaluation and inclusion in the Clinical Trials.gov database.
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In some cases, government agencies, academic institutions, or medical research centers may need to complete this form when seeking to register their clinical trials or studies to comply with regulatory or transparency requirements.
Note: The specific individuals or organizations who need to fill out form au-960 - ctgov may vary depending on the specific regulations, guidelines, or agreements set by the country or institution involved in the clinical trial process. It is crucial to review the requirements and instructions provided by the relevant authorities before completing the form.
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Form AU-960 - ctgov is a form used for reporting financial information related to clinical trials to the U.S. Food and Drug Administration (FDA).
Researchers and organizations conducting clinical trials are required to file form AU-960 - ctgov.
Form AU-960 - ctgov can be filled out electronically on the FDA's website by providing the required financial information.
The purpose of form AU-960 - ctgov is to provide transparency and accountability in financial reporting for clinical trials.
Form AU-960 - ctgov requires reporting of financial information such as funding sources, expenses, and payments related to the clinical trial.
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