Our Customers and Support

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• Pre-Registration Compliance
• Inventories
• Security Review
• Reports
• Prescriptions
• Mock Audits
• Record Keeping
• Theft and Loss Reports
• Prescription Fraud

• Background Investigations
• Registration Applications
• State Compliance
• Drug Security
• Record Keeping
• Drug Audits
• Doctor Shopping awareness

• Registering to become an NTP,  including key elements of the registration process;
• Ordering medication, including how to complete and submit a DEA Form-222 for Schedule II medications and recommendations for establishing an efficient ordering system;
• Receiving medication,  general procedures at the time of delivery, and guidance upon discovering damage/discrepancy to medication shipment;
• Dispensing/administering and destruction of the medication, and procedures for handling the spillage of individual patient doses and accountable losses;
• Recordkeeping, DEA requirements as well as recommendations  and
• Security, including DEA regulatory requirements and recommendations for safes, alarm systems, and accessibility to controlled substance medications.

DEA audits typically take place at random to confirm that your are following the regulations. They can also occur if the DEA receives information that your prescribing, dispensing and distributing patterns are different from other registrants.

DEA inspections are usually routine in nature. However, the DEA may take administrative action against you if they discover that you have violated the CSA. In such cases, your DEA registration may be negatively affected. That’s why you must ensure that you and your team consistently comply with the laws and regulations. If the DEA auditor spots an administrative violation during the inspection, they may issue you a Letter of Admonition. This document will list the issues that the inspector noticed during the audit. You will be granted 30 days to respond to the DEA with pertinent information on how you and your team resolved the problems indicated in the letter.