Of all the major drugs of abuse, only marijuana is available as a natural, harvested product. All of the
others whether illicit drugs
such as cocaine, heroin, methamphetamine, or legitimately produced pharmaceuticals, must be produced or manufactured. Many
problems associated with drug abuse are the result of legitimately-manufactured controlled substances being diverted from their
lawful purpose into the illicit drug traffic.
Drug Enforcement Administration's (DEA) Office of Diversion Control is responsible for two distinct problems: the diversion of controlled pharmaceuticals and the
diversion of controlled chemicals.
Diversion of Controlled Pharmaceuticals
Many of the narcotics, depressants and stimulants manufactured for legitimate medical use are subject to abuse, and have
therefore been brought under legal control. The goal of controls is to ensure that these "controlled substances" are readily
available for medical use, while preventing their distribution for illicit sale and abuse.
Under federal law, all businesses which manufacture or distribute controlled drugs, all health professionals entitled to dispense,
administer or prescribe them, and all pharmacies entitled to fill prescriptions must register with the DEA. Registrants must
comply with a series of regulatory requirements relating to drug security, records accountability, and adherence to standards.
The DEA is obligated under international treaties to monitor the movement of licit controlled substances across
United States borders,
and for issuing import and export permits for that movement. The DEA also devises ways to deal with problems of international
drug diversion.
Diversion cases involve, but are not limited to, physicians who sell prescriptions to drug dealers or abusers; pharmacists who
falsify records and subsequently sell the drugs; employees who steal from inventory; executives who falsify orders to cover
illicit sales; prescription forgers, and individuals who commit armed robbery of pharmacies and drug distributors. At present, the
largest problem results from the criminal activity of physicians and pharmacy personnel.
Diversion of Controlled Chemicals
Most of the drugs in the illicit traffic are products of illicit processing or synthesis. Cocaine, for example, can only be extracted
and converted to its preferred form by using a tremendous quantity of industrial chemicals. Heroin must be synthesized by using
an acetylating agent after the morphine has been extracted from raw, harvested opium. Methamphetamine, PCP, LSD, MDMA
and methaqualone are purely synthetic drugs manufactured from chemical precursors.
Until recently, there were virtually no legal impediments to obtaining the chemicals necessary to manufacture drugs of abuse, no
records required to be maintained for inspection, and no penalties for negligence or willful diversion.
The Chemical Diversion and Trafficking Act of 1988 extended the concept of commodity control to those chemicals most often
used for the manufacture and synthesis of drugs of abuse. With the support of the State Department, DEA pursued the same goal
on the international level. The result was the incorporation of Article 12 into the U.N. Convention Against Illicit Drug Traffic of
1988 (the Vienna Convention). This provision establishes similar controls over a list of 22 critical chemicals commonly diverted
for the production of the major drugs of abuse. In February 1991, the Anabolic Steroid Control Act was passed by Congress.
The act classified 27 named steroids as Schedule III substances under the Controlled Substances Act which DEA administers.
The Office of Diversion consists of diversion investigators, special agents, chemists, pharmacologists, program analysts, and
others. The office's activities include: program priorities and field management oversight; coordination of major investigations;
drafting and promulgating of regulations; establishment of national drug production quotas; design and execution of diplomatic
missions; U.S. obligations under drug control treaties; design and proposal of national legislation; advice and leadership on state
legislation/regulation; legal control of drugs and chemicals not previously under federal control; control of imports and exports of
drugs and chemicals; computerized monitoring and tracking the distribution of certain controlled drugs; providing distribution
intelligence to the states; industry liaison; and program resource planning and allocation.
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