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<td width="271" height="89" align="left" valign="middle" bgcolor="#FFFFFF"><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cylc0Eo" target="_blank"><img alt="GlobalCompliancePanel_Logo" title="GlobalCompliancePanel_Logo" width="254" height="89" border="0"></a></td>
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<td width="81" height="29" align="right" valign="middle"><strong>Date : </strong></td>
<td width="195" align="left" valign="middle"><span>Tuesday, June 14, 2011</span></td>
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<td height="29" align="right" valign="middle"><span><strong>Time : </strong></span></td>
<td align="left" valign="middle">10:00 AM PDT | 01:00 PM EDT</td>
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<td height="29" align="right" valign="middle"><span><strong>Duration : </strong></span></td>
<td align="left" valign="middle">90 Minutes</td>
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<td height="32" align="right" valign="middle"><strong>Price : </strong></td>
<td align="left" valign="middle"><span>$245.00</span></td>
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<td width="428" height="119" align="left" valign="middle" style="padding:10px"><span>Live Webinar</span><br>
<span><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cyle0Eq" target="_blank">How to Survive a DEA Audit</a></span></td>
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<td width="409" height="554" align="left" valign="top"><p><strong>Why Should You Attend</strong>: When DEA Diversion personnel conducts an unannounced inspection to perform an audit on a premise that is registered as a manufacturer or distributor, they generally do not inform the DEA registrant on what steps will be taken during the inspection. In some cases, the registrant is not aware of what information they will need until they ask the registrant. In so many cases, the lack of record-keeping and security requirements will lead to some type of actions from an administrative violations to a civil action that may result in the firm paying thousands of dollars to settle any allegation that were uncovered by DEA personnel. This
presentation will cover all the elements of a DEA inspection and all the record-keeping and security requirements that are expected during that unannounced inspection and will place you in a better situation to understand all the areas of the inspection. By following the outline, you can prepare your firm for that unannounced inspection.</p>
<p><strong>Areas Covered in the Session:</strong></p>
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<li><strong>DEA Office of Diversion Control</strong> - This section will familiarize you with the authority given to the Diversion Group when enforcing the laws and regulations pertaining to controlled substances and regulated chemicals.<br>
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<li><strong>Federal Civil Actions</strong> - Provides a better understanding of the laws and regulations pertaining to the handling of these substances and what specific violations can result in civil actions against a DEA registrant.<br>
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<li><strong>Administrative Actions</strong> - Provides a better insight into the administrative actions that can result from a violation of federal laws and the regulations imposed on the handling of controlled substances and regulated chemicals.<br>
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<li><strong>DEA Computation Chart</strong> - Understanding how an audit is performed by a Diversion Group is very important for any DEA registrant when they arrive at their facility to conduct an unannounced audit and inspection.<br>
</li>
<li><strong>Record-Keeping Requirements</strong> - Covers the records required by the Diversion Group during any unannounced inspection. Records include: biennial inventory, order forms, invoices, quota letters, ARCOS reports, thefts & drugs, power of attorney, and drug destructions. <br>
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<li><strong>Security Requirements</strong> - Covers all the elements of effective security requirements in order to prevent the diversion of any controlled substance and regulated chemical.<br>
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<li><strong>DEA "Know Your Customers" Policy</strong> - Covers the responsibilities placed on a registrant when handling controlled substances and regulated chemicals.<br>
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<li><strong>Sending Documents to DEA</strong> - Learn the methodology and requirements for mailing documents to the local DEA office.</li>
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<p><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cyle0Eq" target="_blank">Click here to register for this webinar</a></p>
<p><strong>Who Will Benefit:</strong>
All regulatory and quality assurance personnel of a manufacturer or distributor registered with DEA to handle controlled substances and regulated chemicals.
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<td width="253" align="center" valign="middle" bgcolor="#0C314C"><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cyle0Eq" target="_blank">Register Now</a></td>
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<td height="20" colspan="2" align="left" valign="middle" bgcolor="#EEEEEE"> Instructor Profile:</td>
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<a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cylf0Er" target="_blank"><img width="32" height="40" border="0"></a></td>
<td width="199" align="left" valign="middle" bgcolor="#EEEEEE"><strong>Carlos M. Aquino</strong><br>
Founder, PharmaDiversion, LLC</td>
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<td height="224" colspan="2" align="left" valign="middle" bgcolor="#EEEEEE"><strong>Carlos M. Aquino</strong> brings 36 years of experience of handling illicit and pharmaceutical controlled substances and regulated chemicals. His testimonial ability, both in federal and state courts, is proof of his investigative experience and skills. Carlos has 12 years of experience working for Philadelphia DEA Diversion Group, which is responsible for initiating prosecutions of those DEA registrants who violate the federal Controlled Substances Act or DEA regulations pertaining to handling these substances. This has included eight years as a Diversion Investigator and four years as a Group Supervisor. During his time at the DEA, he performed
numerous regulatory inspections of manufacturers, distributors, importers/exporters, physicians, researchers, and pharmacies in order to determine their compliance with the federal laws and DEA regulations pertaining to controlled substances in Schedules II through V and regulated chemicals. ...<span><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cylf0Er" target="_blank">more</a></span></td>
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<td width="250" height="25" align="left" valign="middle" bgcolor="#EEEEEE"> Related Products</td>
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<td height="25" align="left" valign="middle" bgcolor="#EEEEEE" style="border-bottom:1px solid #999999"><strong><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cylg0Es" target="_blank">ISO 13485 Gap Analysis Toolkit</a></strong></td>
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<td height="25" align="left" valign="middle" bgcolor="#EEEEEE" style="border-bottom:1px solid #999999"><strong><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cylh0Et" target="_blank">ISO 13485 Quality Manual</a></strong></td>
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<td height="33" align="left" valign="middle" bgcolor="#EEEEEE" style="border-bottom:1px solid #999999"><strong><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cyli0Eu" target="_blank">Intro to ISO 13485 Presentation Materials</a></strong></td>
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<td height="25" align="left" valign="middle" bgcolor="#EEEEEE" style="border-bottom:1px solid #999999"><strong><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cylj0Ev" target="_blank">ISO 13485 Internal Auditor Checklist</a></strong></td>
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<td height="14" align="right" valign="middle" bgcolor="#EEEEEE"><a href="http://info.globalcompliancepanel.com/cgi-bin18/DM/t/he870QnZfv0TOD0Cylk0Ew" target="_blank">more...</a></td>
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<td height="29" colspan="2" align="center" valign="middle">Your Necessity is our Priority</td>
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<td width="680" height="515" align="left" valign="top"><p>It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely benefit from this program.</p>
<p>For more information, please contact the <span><a href="mailto:support@globalcompliancepanel.com" target="_blank">event coordinator</a></span>. We look forward to seeing you at the webinar.</p>
<p>Best regards,<br>
Event-coordinator<br>
GlobalCompliancePanel</p>
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<p><b>About GlobalCompliancePanel</b><br>
GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model for online compliance training by creating a single window of learning opportunities for compliance professionals & providing a forum for expert speakers/panelists to render their services through simplified online training delivery mechanisms. Our commitment is give compliance regulatory training, showcasing of best industry practices & quality enrichment training sessions in a most cost effective manner. Compliance professionals can benefit from a wide range of training sessions, giving a diverse choice of events & all sessions being either Live or recorded stream or in the form of audio CDs. GlobalCompliancePanel portal ensures a secure & cost
effective online environment and also support your E-learning and development on/through our website. Keep track of all webinars arranged for your industry through notifications & event calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for professionals. </p>
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</div><br><br clear="all"><br>-- <br><div>Stevan Gressitt, M.D.<br>Faculty Associate, University of Maine Center on Aging<br>Academic Member, Athens Institute for Education and Research</div>
<div>Athens, Greece</div>
<div>Founding Director, International Institute for Pharmaceutical Safety<br>University of New England, College of Pharmacy<br>Department of Pharmaceutical Sciences <br>Associate Professor of Clinical Psychiatry<br>University of New England, College of Osteopathic Medicine<br>
716 Stevens Avenue <br>Portland, Maine 04103<br><a href="mailto:gressitt@gmail.com" target="_blank">gressitt@gmail.com</a> <br>Cell: 207-441-0291 </div>
<div><a href="http://www.benzos.une.edu/" target="_blank">www.benzos.une.edu</a> </div>
<div><a href="http://www.safemeddisposal.com/" target="_blank">www.safemeddisposal.com</a> <br><br></div><br>