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How to Survive a DEA Inspection Series: For Analytical Labs and Researchers - Webinar By GlobalCompliancePanel

 
  September 11, 2011  
     
 


global compliance panel, Online Training Webinars
2011-09-27


Why should you attend: It is important to understand stringent DEA regulations required of Analytical Labs and Researchers. This training will give them a better insight on steps to take to maintain required record-keeping and effective security in order to prevent illicit use or diversion of any controlled substance. 

The presentation provides effective record-keeping for purchasing and dispensing of controlled substances for testing or research purposes. Inventory, dispensing, usage and disposal records are part of the accountability process in order to comply with stringent DEA regulations. 

Areas Covered in the Session:
  • ROLE OF DEA - familiarize the participant with the authority given to DEA when enforcing federal laws and regulations pertaining to controlled substances.
  • CIVIL ACTIONS - Briefly describes the civil actions and fines imposed by the U.S Attorney’s Office on DEA registered Analytical Labs and Researchers for failures to comply with DEA record-keeping and security regulations.
  • ADMINISTRATIVE ACTIONS - Provides an insight into the administrative actions that results from violations of stringent DEA regulations imposed on Analytical Labs and Research facilities.
  • DEA COMPUTATION CHART - Understanding how the audit process is performed by DEA is important in order for the registrant to know what is expected from employees.
  • RECORD-KEEPING REQUIREMENTS - Covers records required by DEA during any unannounced inspection. Records include: inventory, order forms, invoices, dispensing, usage and disposal in testing, thefts & losses, power of attorney, and drug destructions. 
  • SECURITY REQUIREMENTS - Covers stringent security requirements in order to prevent the diversion of any controlled substance.
  • SENDING DOCUMENTS TO DEA - Learn the methodology and requirements for mailing documents to the local DEA office.
Who Will Benefit:
  • Senior and mid-level Managers
  • Scientists
  • Chemists of DEA registered Analytical Labs
  • Research Facilities
 
 
Organized by: global compliance panel
Invited Speakers:
Carlos M. Aquino 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. 
 
Deadline for Abstracts: 2011-09-27
 
Registration:
Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884

E-mail: webinars@globalcompliancepanel.com
 
   
 
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