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PAR 23 206 NIAID Clinical Trial Planning Grant R34 Clinical 2016-2024

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PAR 23 206 NIAID Clinical Trial Planning Grant R34 Clinical 2016-2024

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>> Stacey Arnold: Hello, my name is Stacey Arnold, and I am a contractor with ICF working as a Results Team Subject-Matter Expert for clinicaltrials.gov. Clinicaltrials.gov is a part of the National Center for Biotechnology Information in the National Library of Medicine at the National Institutes of Health. Today, I will be discussing registering and reporting results to clinicaltrials.gov. During this presentation, I will cover the following topics. First, I will provide a rationale for registering clinical tries and reporting summary level results to clinicaltrials.gov. Next, I will give an overview of registration and results reporting. Then, I will review an online training platform that has been developed to facilitate the registration and reporting processes, the PRS Guided Tutorials. And finally, I will describe an effort that is underway to modernize the clinicaltrials.gov website and PRS database. Why register clinical trials and report summary level results? One of the most

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2016-2024 Form

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Video instructions and help with filling out and completing PAR 23 206 NIAID Clinical Trial Planning Grant R34 Clinical Form

Instructions and help about PAR 23 206 NIAID Clinical Trial Planning Grant R34 Clinical

Find and fill out the correct par 23 206 niaid clinical trial planning grant r34 clinical

Create this form in 5 minutes!

How to create an eSignature for the par 23 206 niaid clinical trial planning grant r34 clinical

How to create an electronic signature for a PDF online

How to create an electronic signature for a PDF in Google Chrome

How to create an e-signature for signing PDFs in Gmail

How to create an e-signature right from your smartphone

How to create an e-signature for a PDF on iOS

How to create an e-signature for a PDF on Android

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