<?xml version="1.0"?>
<law><site_title>Virginia Decoded</site_title><site_url>https://vacode.org</site_url><law_id>67537</law_id><section_number>32.1-69.2</section_number><catch_line>Confidentiality of records; publication; authority of Commissioner to contact parents and physicians</catch_line><edition url="https://vacode.org/2025/" slug="2025" current="TRUE" last_updated="">2025</edition><structure><unit label="title" level="1" order_by="1" identifier="32.1">Health</unit><unit label="chapter" level="2" order_by="1" identifier="2">Disease Prevention and Control</unit><unit label="article" level="3" order_by="1" identifier="8.1">Virginia Congenital Anomalies Reporting and Education System</unit></structure><text>
						<section><p>The <span class="dictionary">Commissioner</span> and all other <span class="dictionary">persons</span> to whom data is submitted pursuant to &#xA7;&#xA0;<a class="law" title="Virginia Congenital Anomalies Reporting and Education System" href="/32.1-69.1/">32.1-69.1</a> shall keep such information confidential. For the purpose of only complying with the provisions of &#xA7;&#xA0;<a class="law" title="Virginia Congenital Anomalies Reporting and Education System" href="/32.1-69.1/">32.1-69.1</a>, hospitals required to report stillbirths, as defined in &#xA7;&#xA0;<a class="law" title="Virginia Congenital Anomalies Reporting and Education System" href="/32.1-69.1/">32.1-69.1</a>, and birth defects to the Virginia Congenital Anomalies Reporting and Education System and provide patient follow-up may view personally identifiable information in the system as approved by the <span class="dictionary">Commissioner</span> and upon receipt by the <span class="dictionary">Commissioner</span> of sworn affirmation from each such <span class="dictionary">person</span> that the confidentiality of the information will be preserved. No publication of information shall be made except in the form of statistical or other studies which do not identify individuals. However, the <span class="dictionary">Commissioner</span> may contact the parents of children identified as having birth defects and their physicians to collect relevant data and to provide them with information about available public and private health care resources.</p></section></text><history>1985, c. 273; 2006, cc. 699, 906; 2015, c. 661.</history><metadata></metadata></law>
