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How to Survive a DEA Inspection Series: Only Manufacturers and Distributors - Webinar By GlobalCompliancePanel

 
  August 10, 2011  
     
 
global compliance panel, Online Training Webinar
2011-08-17


Why should you attend: When DEA Diversion personnel conducts 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 to provide until DEA 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 stringent 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.

Areas Covered in the Session:
  • DEA Office of Diversion Control - This section will familiarize the participant with the authority given to the Diversion Group when enforcing the laws and regulations pertaining to controlled substances and regulated chemicals.
  • Federal Civil Actions - Provides a better understanding of federal laws and regulations pertaining to the handling of those substances and what specific violations can result in civil actions against a DEA registrant.
  • Administrative Actions - 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.
  • DEA Computation Chart - 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.
  • Record-Keeping Requirements - 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. 
  • Security Requirements - Covers all the elements of effective security requirements in order to prevent the diversion of any controlled substance and regulated chemical.
  • DEA "KNOW YOUR CUSTOMERS POLICY" - Covers the responsibilities placed on a registrant when distributing controlled substances and regulated chemicals to their customers.
  • Sending Documents to DEA - Learn the methodology and requirements for mailing documents to the local DEA office.
Who Will Benefit: For marketing purposes, the only targets of this training are Manufacturers and Distributors registered with DEA to manufacture and distribute Schedules I through V controlled substance and regulated chemical products.
 
 
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: 2011-08-17
 
Registration:

2011-08-17

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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