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ClinicalTrials.gov Regulatory Support | Office of Ethics and Compliance
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<a href="/">Home</a> </li> <li class="breadcrumb-item"> ClinicalTrials.gov Regulatory Support </li> </ol> </nav> </div> <div class="layout-content"> <div data-drupal-messages-fallback class="hidden"></div> <div id="block-echo-page-title" class="block block-core block-page-title-block"> <h1 class="page-title"> ClinicalTrials.gov Regulatory Support </h1> </div> <div id="block-echo-content" class="block block-system block-system-main-block"> <div class="node node--type-landing-page node--view-mode-full"> <div class="node__overview"><p>The ClinicalTrials.gov Regulatory Support Team within the Office of Ethics and Compliance provides support to UCSF clinical researchers.</p> </div> <section class="l-container-breakout section-panel background-gray card-panel "> <div class="card-panel__content l-container-offset l-thirds"> <article class="text-card box-shadow"> <h2 class=text-card__title> How the ClinicalTrials.gov Regulatory Team Assists </h2> <a href="/clinicaltrialsgov-regulatory-support" class="text-card__cta"> Assistance with ClinicalTrials.gov </a> </article> <article class="text-card box-shadow"> <h2 class=text-card__title> ClinicalTrials.gov Overview </h2> <div class="text-card__body text-card__overview"> <p> ClinicalTrials.gov is a public registry of research studies involving human subjects. </p> </div> <a href="/clinicaltrialsgov-overview" class="text-card__cta"> General Information on ClinicalTrials.gov </a> </article> <article class="text-card box-shadow"> <h2 class=text-card__title> Registering a Study on ClinicalTrials.gov </h2> <div class="text-card__body text-card__overview"> <p> All Clinical Trials must be registered before enrolling the first subject. </p> </div> <a href="/registering-study-clinicaltrialsgov" class="text-card__cta"> How to Register a Study </a> </article> <article class="text-card box-shadow"> <h2 class=text-card__title> Maintaining a Study Record on ClinicalTrials.gov </h2> <div class="text-card__body text-card__overview"> <p> Record Owners are expected to update their records within 30 days of a change to Overall Recruitment Status external site (opens in a new window) or Completion Dates external site (opens in a new window) and at least once every 12 months. </p> </div> <a href="/maintaining-study-clinicaltrialsgov" class="text-card__cta"> How to Maintain a Study Record </a> </article> <article class="text-card box-shadow"> <h2 class=text-card__title> Reporting Results on ClinicalTrials.gov </h2> <div class="text-card__body text-card__overview"> <p> Results reporting is required within one year of the Primary Completion Date for Applicable Clinical Trials (ACTs) and clinical trials with federal funding and certain other funding sources. </p> </div> <a href="/reporting-results-clinicaltrialsgov" class="text-card__cta"> How to Report Results </a> </article> <article class="text-card box-shadow"> <h2 class=text-card__title> ClinicalTrials.gov Applicable Definitions </h2> <a href="/clinicaltrialsgov-applicable-definitions" class="text-card__cta"> Applicable ClinicalTrials.gov Definitions </a> </article> <article class="text-card box-shadow"> <h2 class=text-card__title> Announcements and Newsletters </h2> <div class="text-card__body text-card__overview"> <p> Essential ClinicalTrials.gov regulatory information for the UCSF Clinical Research community. </p> </div> <a href="/clinicaltrialsgov-announcements-and-newsletter" class="text-card__cta"> Announcements and Newsletters </a> </article> </div> </section> </div> </div> </div> </main> <footer class="footer"> <a href="/" rel="home" title="Office of Ethics and Compliance homepage" class="footer__logo"> <img src="/themes/custom/echo/images/logos/compliance.svg" alt="Office of Ethics and Compliance homepage" height="53" width="189"/> </a> <div class="footer__menus"> <nav aria-label="Footer" class="footer__columns"> </nav> </div><nav class="footer__legal" aria-label="Legal Information"> <p 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