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BEGIN:VEVENT
DTSTART:20170509T080000
DTEND:20170510T173000
SUMMARY:FDA Seminar on Data and Technology
DESCRIPTION:<h2>The Embassy of Denmark in Washington, DC is proud to present again in Copenhagen its unique two-day seminar in collaboration with the U.S. Food and Drug Administration (FDA)</h2>\n<p>&nbsp;</p>\n<h3>Focus on Data &amp; Technology&nbsp;</h3>\n<p>This seminar will focus on the latest developments and use of data and technology in device and drug development in the following sessions:&nbsp;</p>\n<ul>\n    <li>Cybersecurity (latest guidance, NIST framework, ecosystem, expectations, data privacy)&nbsp;</li>\n    <li>Apps working with drugs (what are they, regulatory science/use of, Apps &amp; enforcement)&nbsp;</li>\n    <li>Interoperability (multi-vendor interoperable ecosystem, responsibility and expectations)&nbsp;</li>\n    <li>Drug delivery devices (developments, managing connectivity, regulatory science)&nbsp;</li>\n    <li>Clinical Trials (wearables, commercial grade v. medical grade, assessing endpoints)&nbsp;</li>\n    <li>Medical Device Development Tools (what is it/how to use)&nbsp;</li>\n    <li>CDRH Patient Preference Initiative (gathering information, regulatory decision making)&nbsp;</li>\n    <li>General Wellness (definition, guidance document, affect in device regulation)&nbsp;</li>\n</ul>\n<p>&nbsp;</p>\n<h3>Why Attend?&nbsp;</h3>\n<ul>\n    <li>Opportunity for &ldquo;one-on-one&rdquo; meetings with FDA officials&nbsp;</li>\n    <li>Understand the critical changes to create successful strategies in the USA&nbsp;</li>\n    <li>Benchmark your regulatory strategy against agency requirements&nbsp;</li>\n    <li>Learn and network with your colleagues&nbsp;</li>\n</ul>\n<p>&nbsp;</p>
X-ALT-DESC;FMTTYPE=text/html:<h2>The Embassy of Denmark in Washington, DC is proud to present again in Copenhagen its unique two-day seminar in collaboration with the U.S. Food and Drug Administration (FDA)</h2>\n<p>&nbsp;</p>\n<h3>Focus on Data &amp; Technology&nbsp;</h3>\n<p>This seminar will focus on the latest developments and use of data and technology in device and drug development in the following sessions:&nbsp;</p>\n<ul>\n    <li>Cybersecurity (latest guidance, NIST framework, ecosystem, expectations, data privacy)&nbsp;</li>\n    <li>Apps working with drugs (what are they, regulatory science/use of, Apps &amp; enforcement)&nbsp;</li>\n    <li>Interoperability (multi-vendor interoperable ecosystem, responsibility and expectations)&nbsp;</li>\n    <li>Drug delivery devices (developments, managing connectivity, regulatory science)&nbsp;</li>\n    <li>Clinical Trials (wearables, commercial grade v. medical grade, assessing endpoints)&nbsp;</li>\n    <li>Medical Device Development Tools (what is it/how to use)&nbsp;</li>\n    <li>CDRH Patient Preference Initiative (gathering information, regulatory decision making)&nbsp;</li>\n    <li>General Wellness (definition, guidance document, affect in device regulation)&nbsp;</li>\n</ul>\n<p>&nbsp;</p>\n<h3>Why Attend?&nbsp;</h3>\n<ul>\n    <li>Opportunity for &ldquo;one-on-one&rdquo; meetings with FDA officials&nbsp;</li>\n    <li>Understand the critical changes to create successful strategies in the USA&nbsp;</li>\n    <li>Benchmark your regulatory strategy against agency requirements&nbsp;</li>\n    <li>Learn and network with your colleagues&nbsp;</li>\n</ul>\n<p>&nbsp;</p>

URL:https://www.cachet.dk/da/Calendar/2017/05/FDA-Seminar-2017
DTSTAMP:20260918T015800Z
UID:{89794B83-6C54-4C55-8261-EAC3E0767C51}-20170509T080000-20170509T080000
LOCATION: The seminar will be held in Copenhagen.,  Watch for more information in the coming months. , Seating is limited, so indicate your interest now ,  
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