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Emory University Compliance Program Manual
The number of laws, regulations and policies that impact the multitude of activities carried out at Emory University is enormous, and keeping up with these requirements can be challenging.  Although the Office of Compliance and the Internal Audit Division are separate units with distinct operational charges, both units recognize that a strong compliance program demonstrates the commitment of the University and its employees not only to the laws that govern our activities, but also to the ethical principles at the core of the University as an institute of higher education, research, and health care.  Accordingly, the Office of Compliance and the Internal Audit Division have collaborated on creation of the Emory University Compliance Program Manual as a means of providing faculty and staff members with an overview of the University’s compliance program.  
 
This publication provides faculty and staff members with information about some of the major policies and regulatory requirements that govern employee activities and introduces employees to the strong ethical principles that form the basis for Emory’s mission and work.  We hope this publication will serve both as a useful overview for new employees, and a handy reference guide for current faculty and staff.   
 
The manual is available here


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Follow @EmoryCompliance

Contact us at compliance@emory.edu or 404-727-2398.

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Reporting Concerns Regarding Research Misconduct

Concerns regarding possible Research Misconduct can be reported to Emory’s Research Integrity Officer, Kris West at 404-727-2398 or via the Trust Line.  The Trust Line can accessed by calling 1-888-550-8850 or via the Trust Line Online reporting tool: http://www.mycompliancereport.com/EmoryTrustLineOnline.  For more information on Research Misconduct click here.  Additional information regarding the Trust Line is available here.

Authorship Issues:

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Controlled Substances and Dangerous Drugs must be secured and a record of their use for research must be kept.  More resources related to Controlled Substances and Dangerous Drugs, as well as a link to full lists of these drugs are available here.

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This notice affects both Researchers (renewal form 225a) and Practitioners (renewal form 224a). The notice, “Change in DEA Registration Application Renewal Notification Reminder”, can be viewed at: 极迅加速器-更快更稳的网游手游免费加速器:2021-6-15 · 极迅加速器是一款免费的网络网游游戏加速器,支持上千款热门游戏加速器免费下载,包括吃鸡加速器,steam加速器,英雄联盟加速器,GTA5加速器等.新用户免费试用!有效解决玩家在网络游戏中遇到的延时过高,登录困难,容易掉线等问题,选免费游戏加速器,就选极迅网络游戏加速器.

Information Resource for FDA Regulated Studies and  Sponsor-Investigator Studies

The Office of Compliance assists investigators, coordinators and the Emory research community by providing education and consultation regarding regulatory requirements, compliance obligations and best practices.  Specific information, forms and templates are available for Sponsor Investigators conducting 安卓坚果加速器 and 坚果加速器吧.