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<NewsItem contentIssues="false" id="17326" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/17326">
<Title>Attend an animal care webinar</Title>
<Body>
<![CDATA[
    <div class="html-content">The ORPC has secured a space and is hosting the viewing a Public
    Responsibility in Medicine and Research (PRIM&amp;R) webinar entitled " The
    IACUC's Role in Environmental Enrichment Programs" on Tuesday, October 9,
    2012 from 1:00 to 2:30 pm.<br><p></p>
    
    <p>For more information and if you'd like to attend, please
    click this link <a href="http://my.umbc.edu/groups/compliance/events/14171" rel="nofollow external" class="bo">http://my.umbc.edu/groups/compliance/events/14171</a>
    to register.</p></div>
]]>
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<Summary>The ORPC has secured a space and is hosting the viewing a Public Responsibility in Medicine and Research (PRIM&amp;R) webinar entitled " The IACUC's Role in Environmental Enrichment Programs" on...</Summary>
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<PostedAt>Fri, 05 Oct 2012 16:32:03 -0400</PostedAt>
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<NewsItem contentIssues="false" id="17312" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/17312">
<Title>NSF guidance updates re: animal use and use</Title>
<Body>
<![CDATA[
    <div class="html-content"><p>NSF has updated the Grant Proposal Guide (GPG) and the <span>Award &amp; Administration Guide (AAG</span>),
    with changes effective January 14, 2013 providing clarification and updated
    guidance on proposals and awards involving vertebrate animals. These updates
    now contain references to the review of wildlife research protocols, the IACUCs
    role in the review and approval of such research, and the processes to follow
    for UMBC investigators to follow when submitting and/or receiving funding from
    the NSF. </p>
    
    <p>Completed versions of the GPG and AAG are available at <a href="http://www.nsf.gov/bfa/dias/policy/" rel="nofollow external" class="bo">http://www.nsf.gov/bfa/dias/policy/</a>;
    attached of the extracted pages related to vertebrate animals. Please contact
    the ORPC with any questions.</p></div>
]]>
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<Summary>NSF has updated the Grant Proposal Guide (GPG) and the Award &amp; Administration Guide (AAG), with changes effective January 14, 2013 providing clarification and updated guidance on proposals and...</Summary>
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<PostedAt>Fri, 05 Oct 2012 10:53:51 -0400</PostedAt>
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<NewsItem contentIssues="false" id="17089" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/17089">
<Title>Emergency Preparedness Training</Title>
<Tagline>Staying safe on campus during an emergency</Tagline>
<Body>
<![CDATA[
    <div class="html-content">Helpful seminar for all investigators, particularly in the research labs. Go to <a href="http://my.umbc.edu/events/13728" rel="nofollow external" class="bo">http://my.umbc.edu/events/13728</a> to sign up. </div>
]]>
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<Summary>Helpful seminar for all investigators, particularly in the research labs. Go to http://my.umbc.edu/events/13728 to sign up. </Summary>
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<PostedAt>Wed, 26 Sep 2012 11:07:26 -0400</PostedAt>
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<NewsItem contentIssues="false" id="17086" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/17086">
<Title>Export Controls - NCURA Youtube Tuesday</Title>
<Body>
<![CDATA[
    <div class="html-content"><p>Export controls, the federal regulations that oversee how certain information, services and products are provided to foreign nationals and countries, is a complicated issue for Sponsored Programs and PIs but also for department administrators in the funding award process.</p><p><br></p><p>The recent National Council of University Research Administrators (NCURA) YouTube Tuesday video, “4 Key Concepts When Addressing Export Controls” provides information on what to keep in mind when export controls are part of an award.</p><p><br></p><p>See <a href="http://www.youtube.com/user/ncura1959" rel="nofollow external" class="bo">http://www.youtube.com/user/ncura1959</a> for the video. For more information about UMBC’s export control process, go to <a href="http://my.umbc.edu/groups/compliance/documents/164" rel="nofollow external" class="bo">http://my.umbc.edu/groups/compliance/documents/164</a>. </p></div>
]]>
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<Summary>Export controls, the federal regulations that oversee how certain information, services and products are provided to foreign nationals and countries, is a complicated issue for Sponsored Programs...</Summary>
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<PostedAt>Wed, 26 Sep 2012 09:55:59 -0400</PostedAt>
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<NewsItem contentIssues="false" id="16257" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/16257">
<Title>September is National Preparedness Month</Title>
<Body>
<![CDATA[
    <div class="html-content"><div>September is National Preparedness Month. A series of disaster/crisis webinars sponsored by the US Small Business Administration and the Federal Emergency Management Agency on various topics will be presented each Wednesday in September at 2:00 PM EDT. Information in these seminar may be useful for our facility personnel</div><div><br></div><div>Topics include: </div><div>September 5: Ten Steps to Prepare Any Organization for Disaster</div><div>September 12: Prepare Your Employees &amp; Protect Your Organization</div><div>September 19: Utilizing Social Media During a Crisis</div><div>September 26: Surviving a Crisis, Large or Small: Real Life Lessons Learned</div><div><br></div><div><br></div><div>Register for the webinars below</div></div>
]]>
</Body>
<Summary>September is National Preparedness Month. A series of disaster/crisis webinars sponsored by the US Small Business Administration and the Federal Emergency Management Agency on various topics will...</Summary>
<Website>http://www2.agilityrecovery.com/npm</Website>
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<PostedAt>Wed, 29 Aug 2012 09:55:34 -0400</PostedAt>
<EditAt>Wed, 29 Aug 2012 09:56:03 -0400</EditAt>
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<NewsItem contentIssues="false" id="16121" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/16121">
<Title>Guidance and clarifications from NIH</Title>
<Body>
<![CDATA[
    <div class="html-content"><p><span>The NIH released two new guidance and clarification documents of existing policies related to research
    approval and grant resubmissions.</span></p>
    
    <p><span> </span></p>
    
    <p><span>One notice (<a href="http://grants.nih.gov/grants/guide/notice-files/NOT-OD-12-129.html" rel="nofollow external" class="bo">http://grants.nih.gov/grants/guide/notice-files/NOT-OD-12-129.html</a> ) outlines the process for requesting approval in the event that research under
    an active NIH award has changed to involve an increased risk to human subjects.
    If changes occur within a UMBC IRB approved protocol, where </span><span>prior NIH approval is required before implementation</span>, contact the <span>Office for Research Protections and Compliance (at 5-2737 or <a href="mailto:compliance@umbc.edu" rel="nofollow external" class="bo">compliance@umbc.edu</a>)  as soon as possible so that we may assist in
    the processing and review of protocol modification documents.</span><span></span></p>
    
    <p><span> </span></p>
    
    <p><span>A second notice (<a href="http://grants.nih.gov/grants/guide/notice-files/NOT-OD-12-130.html" rel="nofollow external" class="bo">http://grants.nih.gov/grants/guide/notice-files/NOT-OD-12-130.html</a>)
    describes the approval process for the addition of human subjects research to
    projects that were originally awarded without definitive plans for human
    subjects research described in the grant application. The UMBC IRB has issued
    guidance that may assist investigators in situations described in this second notice.
    Investigators may request planning phase administrative approval to obtain IRB
    approval. Please see</span><span> <a href="http://www.umbc.edu/research/ORPC/irb_forms.html#planning" rel="nofollow external" class="bo">http://www.umbc.edu/research/ORPC/irb_forms.html#planning</a>
    for more information.</span><span></span></p></div>
]]>
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<Summary>The NIH released two new guidance and clarification documents of existing policies related to research approval and grant resubmissions.         One notice...</Summary>
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<PostedAt>Fri, 24 Aug 2012 14:39:14 -0400</PostedAt>
<EditAt>Fri, 24 Aug 2012 14:40:47 -0400</EditAt>
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<NewsItem contentIssues="false" id="15874" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/15874">
<Title>Revisions to NASA research misconduct policy</Title>
<Body>
<![CDATA[
    <div class="html-content"><p>NASA updates its research misconduct policy which will go
    into effect on September 28, 2012 - <a href="https://www.federalregister.gov/articles/2012/07/30/2012-18435/research-misconduct" rel="nofollow external" class="bo">https://www.federalregister.gov/articles/2012/07/30/2012-18435/research-misconduct</a></p><p><br></p><p>A list of of federal agency policies is found at <a href="http://www.umbc.edu/research/ORPC/RCRpolicyregs.html" rel="nofollow external" class="bo">http://www.umbc.edu/research/ORPC/RCRpolicyregs.html</a></p></div>
]]>
</Body>
<Summary>NASA updates its research misconduct policy which will go into effect on September 28, 2012 - https://www.federalregister.gov/articles/2012/07/30/2012-18435/research-misconduct     A list of of...</Summary>
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<NewsItem contentIssues="false" id="15600" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/15600">
<Title>Guidelines for Reporting Sensitive Information</Title>
<Body>
<![CDATA[
    <div class="html-content"><p><span>During the course of certain
    types of research, investigators may discover sensitive information about
    subjects that is not related to the study itself which would be reported the
    appropriate authorities</span> (e.g., use of illegal substances or suspected
    child abuse). It is important for investigators to be aware of the signs of
    child abuse, reporting responsibilities, and where to report any suspicion. </p>
    
    <p><span>The IRB has developed
    <a href="http://www.umbc.edu/research/ORPC/IRBspecialtopics.html#sensitive" rel="nofollow external" class="bo">guidance for investigators</a> describing reporting responsibilities as described by <a href="http://umbc.edu/ogc/hr/faq_usm.html" rel="nofollow external" class="bo">UMBC's implementation</a> of the USM Board of Regents </span><span>Policy
    on the Reporting of Suspected Child Abuse and Neglect.</span></p>
    
    <p><span>Application forms and consent documents
    have been modified to reflect this guidance. Please see ORPC’s<a href="http://my.umbc.edu/groups/compliance" rel="nofollow external" class="bo">Human Subjects
    page</a> for more information.</span></p></div>
]]>
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<Summary>During the course of certain types of research, investigators may discover sensitive information about subjects that is not related to the study itself which would be reported the appropriate...</Summary>
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<PostedAt>Fri, 06 Jul 2012 10:04:11 -0400</PostedAt>
<EditAt>Fri, 06 Jul 2012 10:07:17 -0400</EditAt>
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<NewsItem contentIssues="false" id="15544" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/15544">
<Title>Planning for human subjects use</Title>
<Body>
<![CDATA[
    <div class="html-content"><div><span><div>At times principal investigators will plan research projects that will eventually lead to the submission of grant applications where human subjects use are planned in future but have not been finalized, or when a PI received a "just-in-time" notice from a granting agency and is requesting documentation of IRB approval.</div><div><br></div><div>An investigator may request review of a project for a planning only and that a submission of an IRB application for the complete study is required prior to initiating the research.</div><div><br></div><div>The IRB has issued <a href="http://www.umbc.edu/research/ORPC/irb_forms.html#planning" rel="nofollow external" class="bo">guidance</a> to address this topic.</div><div><br></div></span></div></div>
]]>
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<Summary>At times principal investigators will plan research projects that will eventually lead to the submission of grant applications where human subjects use are planned in future but have not been...</Summary>
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<NewsItem contentIssues="false" id="15360" important="false" status="posted" url="https://beta.my.umbc.edu/groups/compliance/posts/15360">
<Title>Draft Guidance from the OHRP</Title>
<Body>
<![CDATA[
    <div class="html-content"><div>The Office for Human Research Protections (OHRP) has recently released a draft guidance document regarding the transfer of a previously IRB approved research project to a new IRB or new institution.</div><div><br></div><div>This guidance, when finalized, will help investigators, staff and the IRB understand what is required when such projects are transferred.</div><div><br></div><div>The ORPC staff will be working with the IRB over the next several months to develop procedures for this process and will inform the campus community of the progress. In the meantime, please review these links for more information.</div><div><br></div><div><div>Federal Register notice -  <a href="http://www.gpo.gov/fdsys/pkg/FR-2012-06-12/html/2012-14287.htm" rel="nofollow external" class="bo">http://www.gpo.gov/fdsys/pkg/FR-2012-06-12/html/2012-14287.htm</a></div><div><br></div><div>Draft guidance - <a href="http://www.hhs.gov/ohrp/newsroom/rfc/transferdraftdoc.html" rel="nofollow external" class="bo">http://www.hhs.gov/ohrp/newsroom/rfc/transferdraftdoc.html</a></div></div></div>
]]>
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<Tag>irb</Tag>
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<PostedAt>Wed, 20 Jun 2012 14:45:36 -0400</PostedAt>
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