updates from the dea - nascsanascsa.org/conference2018/presentations/arnold.pdf · updates from the...
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Updates from the DEA
James Arnold, ChiefLiaison Section/DPL Diversion Control Division
National Association of
State Controlled Substance AuthoritiesScottsdale, Arizona
Tuesday, October 30, 2018
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Opioid Drug Treatment
The Comprehensive Addiction and Recovery Act of 2016
“CARA”July 22, 2016
Public Law 114-198
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Opioid Drug TreatmentQualifying Practitioners(Qualifying Physicians)(DATA Waived Doctors)
Qualifying Other Practitioners(Nurse Practitioners)(Physician Assistants)
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Opioid Drug TreatmentQualifying Practitioners
(30, 100, 275 Patients)
Qualifying Other Practitioners(30, 100 Patients)
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Dispensing Buprenorphine
5
• Administer, Dispense, and Prescribe as Allowed by Federal and State Law and Regulations.
• “Active Script, Active Patient”
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6
0
2,000
4,000
6,000
8,000
10,000
12,000
14,000
16,000
2009 2010 2011 2012 2013 2014 2015 2016 2017
Total Prescriptions Filled: Buprenorphine 2009-2017
IMIMSIMS IMS Data
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*As of October 25, 2018: DEA Data
Opioid Treatment Programs (OTPs)
1,375 1,4181,509
1,5951,669
0
200
400
600
800
1,000
1,200
1,400
1,600
1,800
2014 2015 2016 2017 2018
Opioid Treatment Program (OTP) Totals
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4
25
166
78
28
82
4
13
4
71
17DC 5
43
22
45 7
19
10
10
83
86
10
45
16
17
5
4
71
3
4
9
16
4116
130
19
3893
19
6
83
1521
1
95
1642
1
1027
20
9
0
DEA Registered Opioid Treatment Programs (OTP)
Drug Enforcement Administration, Diversion Control Division Updated September 18, 2018Total: 1,662
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9*As of October 25, 2018 (NPs and PAs as of 01/01/2017)
DEA Registered Qualifying Practitioners
14,778
27,719
52,375
0
10,000
20,000
30,000
40,000
50,000
60,000
2010 2015 2018
Data Waived Physician (DWP)/Qualifying Practitioner Totals
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265
538
5228 9221006
200
157
179
885
174
DC 200
1009
956
996 163
804
178
538
2704
1637
694
1328
592
580
243
138
1304
70
99
425
590
1496364
4988
372
25162725
904
458
418
847557
71
1680
607858
3421920
702
406
71
DEA Registered Qualifying Practitioners
Drug Enforcement Administration, Diversion Control Division Updated 9/18/2018Guam: 2
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Qualifying Practitioners (US)
• Practitioner DW-30 30,293• Practitioner DW-100 9,535• Practitioner DW-275 4,639• Nurse Practitioner DW-30 6,285• Physician Assistant DW-30 1,623
As of October 25, 2018
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New Regulatory Clarity
• Pending New Regulation Clarity – EPCS– Mobile Treatment Vans– Mobile Doctors– Partial Fill Regulations– One Page DEA Form 222– Special Registration for Telemedicine– EMS
12
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Options for Hospitals
13
21 C.F.R. 1306.07:
• Register as an NTP
• Three Day Rule (Withdrawal)
• Incidental Adjunct to Medical/Surgical Treatment
• DATA Waived (Qualifying Practitioner)
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Revised Manuals
Narcotic Treatment Manuals
Practitioners Manual
Pharmacy Manual
Researcher’s Manual
14
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National Emergencies
DEA Registrants
Domestic or International disasterssuch as Hurricanes, Earthquakes, Floods, Tornadoes, and Typhoons.
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National Emergencieshttp://www.DEAdiversion.usdoj.gov
At the Above Listed Homepage Click on Tab at the Bottom of the Home Page Titled:
Click on: [email protected]
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Factory Visit Photos
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Domestic Control of MarihuanaFor marijuana to be moved from Schedule I to another schedule, the substance/drug requires an accepted medical use.The definition of currently accepted medical use was litigated, Alliance for Cannabis Therapeutics v DEA (D.C. Cir 1994)
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“Five Part Test for Currently Accepted Medical Use”
Five Part test:
1) The drug’s chemistry must be known and reproducible;
2) There must be adequate safety studies;
3) There must be adequate and well-controlled studies proving efficacy;
4) The drug must be accepted by qualified experts; and
5) The scientific evidence must be widely available
Marinol - Yes
Marijuana - No
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• State laws, anecdotal reports, position statements do not fulfill these criteria.
• The U.S. Department of Health and Human Services (HHS) is the sole domestic entity with the authority to approve medications for use by humans and animals.
Domestic Control of Marihuana
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Marihuana
is
a
Schedule I Controlled Substance
Under Federal Law
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Recent Examples of Drugs Participating in the Process
• Drug sponsor conducted clinical trials and collected the information required of the FDA
• DEA registered the researchers and the sponsor conducted their studies
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Epidiolex®
• June 25, 2018
• FDA Approved Epidiolex®
• 1st Pharmaceutical Grade CBD Product derived from Cannabis in an FDA approved medication.
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Epidiolex®• Approved for the treatment of
Lennox-Gastaut syndrome Dravet syndrome
• Two serious and rare forms of epilepsy that appear at an early age.
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Epidiolex®Schedule V
Approved by FDA onMonday, June 25, 2018
Scheduled by DEA onFriday, September 28, 2018
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Placement in Schedule V of Certain FDA-Approved Drugs
29
FDA-approved drugs that contain CBD
derived from cannabis and no more than 0.1 percent
tetrahydrocannabinols into Schedule V
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MarihuanaDEA continues to support legitimate medical and scientific research on marijuana and its derivatives, extracts and synthetic versions.
To date, the DEA has not denied any application to conduct FDA approved research with marijuana.
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Marihuana• As of October 10, 2018, DEA has
approved a total of 692 researchers nationwide to perform research with Schedule I controlled substances.
• Approximately 499 of those researchers are conducting research with marijuana, marijuana extracts, and/or THC.
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What’s New?
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H.R.6
SUPPORT for Patients and Communities Act
115th Congress (2017-2018)
October 24, 2018
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Substance Use-Disorder Prevention that Promotes
Opioid Recovery and Treatment for Patients and Communities Act
or the SUPPORT for Patients and
Communities Act
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35
I. Provisions Amending the Controlled Substances Act
II. Provisions Requiring the Promulgation of DEA Regulations
III. Provisions Requiring Consultation with DEA
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Provisions Amending
the Controlled Substances Act
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Section 3204:
37
Delivery of a Controlled Substance by a Pharmacy to be Administered by Injection or Implantation
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1. Amends the CSA to allow a pharmacy to deliver a controlled substance directly to a practitioner to be administered to a specific patient for injection or implantation maintenance or detoxification treatment. 2. Will allow delivery to a practitioner at the location listed on the practitioner's certificate of registration 3. 14 Days to Administer 38
Section 3204:
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DEA has already provided exceptions for some substances (for the treatment of Opioid Addiction):• Investigational buprenorphine product RBP-
6000Indivior
• Probuphine (buprenorphine) implantBraeburn Pharmaceuticals
• Implanted intraspinal pumpsAdvanced Infusion Solutions (AIS)
Delivery to a Practitioner’s Office
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New Products
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New Products
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Section 3222:
43
Disposal of Controlled Substances of a Hospice Patient by Employees of a Qualified Hospice Program
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• Three specific circumstances when an employee of a qualified hospice program may assist with disposal of the controlled substances:
1. The disposal occurs after the death of a person receiving hospice care
2. The controlled substance is expired 44
Section 3222:
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3. Change of care of the patient only in instances where the employee is a DEA registrant and the practitioner of the patient
• Disposal shall occur onsite and in accordance with all applicable Federal and State law
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Chapter 7:
46
Using Data to Prevent Opioid Diversion
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• Amends the CSA to provide drug manufacturers and distributors with access to anonymized information through the Automated Reports and Consolidated Ordering System (ARCOS) to assist in identifying, stopping, and reporting suspicious orders of opioids.
47
Chapter 7:
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• The following anonymized data will be made available via ARCOS Quarterly
1. Total Number of competitors who have sold a particular controlled substance to a prospective customer (pharmacy or practitioner)
2. Quantity and type of opioids distributed
48
Chapter 7:
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“anonymized”
• Make anonymous
• Remove identifying particulars so that the original source cannot be known
49
“Anonymized”
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• A bi-annual reporting requirement to provide a standardized report to regulatory, licensing, attorneys general, and law enforcement agencies of States.
• Nothing in this chapter should be construed to absolve a DEA registrant from the responsibility of identify and report suspicious orders 50
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Chapter 8:
51
Opioid Quota Reform
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• Amends the CSA to strengthen DEA’s discretion in setting opioid quota by codifying changes outlined in the April 2018 notice of proposed rulemaking and outlines an annual reporting requirement to congress regarding manufactures and aggregate production quota increases.
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Chapter 8:
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• DEA may establish APQ, MQ, and/or PQ in terms of pharmaceutical dosage forms to avoid the overproduction, shortages, or diversion of a controlled substance
-MQ deadline changed from October 1 to December 1-Estimated amount of diversion shall be considered when setting APQ, MQ, and/or PQ
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Chapter 8:
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• Congressional annual reporting requirement due:
-For any year for which the approved APQ for a covered controlled substance is increased-An anonymized count of manufactures issued MQ and number of manufactures who received increases in MQ from previous year
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Chapter 8:
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Chapter 9:
Preventing Drug Diversion
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• Requires DEA to establish a centralized database for collecting reports of suspicious orders within one year of enactment of this law.
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Chapter 9:
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• Defines and adds the term ‘suspicious order’ to the CSA
• DEA shall establish a centralized database for collecting reports of suspicious orders
• A standardized report to be made available to regulatory, licensing, attorneys general, and law enforcement agencies of States within a reasonable period of time
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Chapter 9:
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• A call for State AG’s to provide access to DEA regarding PDMP data
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Chapter 9:
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Section 3201:
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Allowing for More Flexibility with Respect to Medication-Assisted Treatment for Opioid Use Disorders
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• Amends the CSA to increase the number of patients a DATA waived practitioner may treat and eliminates the time limitation for specific practitioner types to be considered a ‘Qualified Practitioner’.
• Permanently codifies the 275 patient limit for DATA waived practitioners
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Section 3201:
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• Eliminates time limitation (Sunset Provision) for nurse practitioners and physician assistants to become qualifying practitioners
• Imposes a 5 year time limitation (Sunset Provision) on clinical nurse specialists, registered nurse anesthetists, and certified nurse midwifes to become qualifying practitioners
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Section 3201:
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Section 3202:
Medication-Assisted Treatment for Recovery from Substance Use Disorder
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Section 3202: • Amends the CSA to expand the type of
practitioners that may obtain a DATA wavier with respect to medication-assisted treatment (MAT).
• A physician who graduated from an accredited school of allopathic medicine or osteopathic medicine may obtain a DATA wavier with respect to medication-assisted treatment (MAT)
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Provisions Requiring the
Promulgation of DEA Regulations
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Section 2003:
Every Prescription Conveyed Securely
• Requires updated DEA regulations for thebiometric component of multifactor authentication with respect to electronic prescriptions of controlled substances (EPCS).
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Chapter 4:
Regulations Relating to a Special Registration for Telemedicine
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• Requires a DEA regulation that contains both the limited circumstances and procedure for obtaining a special registration for telemedicine.
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Chapter 4:
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Provisions Requiring Consultation
with DEA
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Section 3212:
• Programs and Materials for Training on Certain Circumstances Under which a Pharmacist may Decline to Fill a Prescription
• HHS, in consultation with DEA, shall develop materials explaining circumstances under which a pharmacist may decline to fill a prescription for a controlled substance.
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Section 8215:
• Provider Education
• DEA, in coordination with HHS, shall provide a report outlining additional steps recommended to limit the over-prescribing of opioids by medical practitioners and clearly identify how DEA can help to regulate registrations for the dispensing of controlled substances.
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A Final Note
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The mission of the Diversion Control Division is to prevent, detect, and investigate the diversion of pharmaceutical controlled substances and listed chemicals from legitimate channels of distribution…
Mission
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… while ensuring an adequate and uninterrupted supply of controlled substances to meet legitimate medical, commercial,and scientific needs.
Mission
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The DEA is primarily responsible for Enforcing the CSA
Providing for the Public Health and Safety
Mission
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21 C.F.R. § 1306.04 (a)
A prescription for a controlled substance to be effective must be issued for a legitimate medicalpurpose by an individual practitioner acting in the usual course of his professional practice.
75U.S. Drug Enforcement AdministrationDiversion Control Division
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Thank You
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Contact InformationJames Arnold, ChiefLiaison Section/DPLDrug Enforcement Administration8701 Morrissette DriveSpringfield, Virginia 22152
202-353-1414 (Office)