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    <pubDate>Wed, 15 Apr 2026 22:18:41 GMT</pubDate>
    <dc:date>2026-04-15T22:18:41Z</dc:date>
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      <title>Safety Reporting in Clinical Trials</title>
      <link>https://hdl.handle.net/20.500.14356/2544</link>
      <description>Title: Safety Reporting in Clinical Trials
Authors: Porasuphatana, Supatra
Abstract: Drug Development: Regulatory Reviews
Description: Presentation</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
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      <dc:date>2024-01-01T00:00:00Z</dc:date>
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      <title>Protocol Amendment Decision: IRB's Role</title>
      <link>https://hdl.handle.net/20.500.14356/2543</link>
      <description>Title: Protocol Amendment Decision: IRB's Role
Authors: Chatsiricharoenkul, Somruedee
Description: Presentation.</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
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      <dc:date>2024-01-01T00:00:00Z</dc:date>
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      <title>Post Approval Continuing Processes: Site Visit</title>
      <link>https://hdl.handle.net/20.500.14356/2542</link>
      <description>Title: Post Approval Continuing Processes: Site Visit
Authors: Prayoonwiwat, Naraporn; Bunsi, Adun
Abstract: NA
Description: Presentation</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
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      <dc:date>2024-01-01T00:00:00Z</dc:date>
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      <title>Conducting Site Visits</title>
      <link>https://hdl.handle.net/20.500.14356/2541</link>
      <description>Title: Conducting Site Visits
Authors: Jimeno, Cecilia A.
Abstract: Outline of Discussion&#xD;
What is a site visit by an REC?&#xD;
Reasons for RECs to do site visits &amp; criteria for selection of sites&#xD;
Procedures involved in the site visit: composition, preparation, conduct, reporting
Description: Presentation</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
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