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Drug Enforcement Agency

Drug Enforcement Administration

Drug Enforcement AdministrationWhat is the Drug Enforcement Administration (DEA)?

The Drug Enforcement Administration is a federal law enforcement agency within the United States Department of Justice. The Drug Enforcement Administration, better known as the DEA, is tasked with combating drug smuggling and use within the borders of the United States of America. Not only is the Drug Enforcement Administration regarded as the leading agency for domestic enforcement of the Controlled Substances Act, but it also maintains the sole responsibility for coordinating and subsequently pursuing U.S. investigations overseas.

The Drug Enforcement Administration was officially formed on July 1 of 1973. The administration was established by the passing of the Reorganization Plan; a full-fledged effort to organize the federal agencies responsible for diminishing the adverse effects of drugs on American Society. The legislation, which ultimately created the Drug Enforcement Administration, was signed by President Richard Nixon and proposed the creation of a single federal agency to enforce the federal drug laws and consolidate, as well as coordinate, the government’s expansive drug control policies.

The preceding agencies of the DEA were the Bureau of Narcotics and Dangerous Drugs and the Office of Drug Abuse Law Enforcement. The Drug Enforcement Administration, to mitigate the dangers associated with drug use and to lessen the supply of deadly drugs in the United States, employees nearly 11,000 agents and operates with an annual budget of approximately $2.5 billion.

In 2005, the Drug Enforcement Administration was successful in seizing over $1.4 billion in drug trade related assets and over $475 million worth of drugs. That being said, according to the White House’s Office of Drug Control Policy, the total value of all drugs sold in the United States is thought to exceed $65 billion per year—making the DEA’s efforts to intercept and thwart the flow of drugs into the country less than 1% effective.

The Drug Enforcement Administration is a federal agency under the jurisdiction of the United States Department of Justice responsible for the bulk of criminal investigations, analysis, and collection of information concerning drug-related criminal activity; working closely with related branches of the Department of Justice, the DEA both furnishes and receives vital intelligence from the Federal Bureau of Investigation (FBI) with regard to both individuals charged with committing drug-related offenses, as well as the investigation of individuals alleged to be participatory in those crimes.
The Drug Enforcement Administration is responsible the regulation and handling of a variety of matters concerning drug-crimes, as well as the vast array of illegal drug use existing on both national and international levels:



How is the Drug Enforcement Administration Organized?
The Drug Enforcement Administration is headed by an Administrator who is formally appointed by the President of the United States and confirmed by the U.S. Senate. The administrator is required to report to the Attorney General through the Deputy Attorney General. The individual is assisted by a Deputy Administrator, as well as the Chief of Operations, the Chief Inspector and three Assistant Administrators.

The headquarters of the Drug Enforcement administration are located in Arlington, Virginia, directly across from the Pentagon. The administration maintains its own training academy located on the United States Marine Corps base at Quantico, Virginia. In total, the Drug Enforcement Administration maintains 21 domestic field divisions with 227 field offices as well as 86 international offices located in 62 countries.
Drugs and Controlled Substances
On one hand, the DEA is responsible for the criminal investigation and prevention of crimes involving both the usage and sales of illegal narcotics – on the other hand, the DEA undertakes regulatory and preventative measures to deride the misuse of controlled substances – controlled substances are classified as drugs whose legality is contingent on both authorized prescription and lawful usage.
Within the States where Medical Marijuana is legalized, an individual patient prescribed Medical Marijuana is permitted to undertake its usage in the event that the DEA has approved of the prescription and need; however, an individual using Marijuana recreationally – absent of a prescription – will be in violation of applicable legislature 


Drug Enforcement Administration Quick Facts
The following details outline the administration of the Drug Enforcement Administration:
The Drug Enforcement Administration was founded on July 1st, 1973
The headquarters of the Drug Enforcement Administration are located in Virginia
The agency executive of the Drug Enforcement Administration is Michelle Leonhart

Agencies Associated with the Drug Enforcement Administration
Government agencies are defined as organizations, councils, and offices operating under the jurisdiction of the Federal Government of the United States of America; each federal agency retains specific administrative jurisdiction over specific facets latent within the operations of the United States Government:

The USDOJ and the Drug Enforcement Administration
The Department of Justice is a federal agency within the Executive Branch of the government responsible for the supervision of the Drug Enforcement Administration, which is considered to be a sub division within the USDDOJ; the Department of Justice undertakes all manners of criminal activity existing on a national level, which includes drug-crimes occurring on both foreign and national levels.

The Diversion Control Program and the DEA
The Diversion Control Program is a branch of the Drug Enforcement Administration (DEA) responsible for the assurance that controlled substances undergo legal verification, validation, and substantiation of the prescription of drugs and pharmaceuticals classified as controlled substances.

Drug Enforcement Administration Legality
Administrative Law is the legal field associated with events and circumstances in which the Federal Government of the United States engages its citizens, including the administration of government programs, the administration and operation of government agencies.

What you must know about FDA Jobs

What you must know about FDA JobsFDA Defined:

The Food and Drug Administration is a Federal agency that operates within the United States Department of Health and Human Services. The Food and Drug Administration is one of the country’s federal executive departments and is responsible for protecting and promoting public health through the supervision and regulation of tobacco products, food safety dietary supplements, prescription, as well as over-the-counter pharmaceutical drugs, biopharmaceuticals, vaccines, medical devices, electromagnetic radiation emitting devices, cosmetics, veterinary products and vaccines.

In addition to the regulation over the aforementioned products, the Food and Drug Administration enforces other laws, most notably Section 361 of the Public Health Service Act and associated legislation, which may or may not be related to food and drugs. In this format, the Food and Drug Administration is responsible for the regulation of sanitation requirements on interstate travel and the control of disease on products ranging from household pets to the donation of sperm intended for assisted reproduction.

Why are FDA Jobs Important?

FDA jobs are a crucial aspect of the United States Federal Government; FDA jobs are responsible for protecting the United States’ general public’s safety and health through the implementation of regulations and standards regarding medications, medical devices, cosmetics, food, vaccinations, tobacco and dietary supplements. As a result of this seemingly all-encompassing regulatory responsibility, the FDA imposes various regulations in a number of areas.

From FDA regulations concerning the packaging of products to the administration of safe drugs, all FDA regulations must be satisfied by the producers and manufacturers of food, cosmetics, drugs, vaccines, medical supplies and various other consumer products in the United States. Failure to comply with these FDA regulations will result in felony charges (placed on the producer, distributor or manufacturer of the aforementioned goods) or the institution of an FDA product recall.

What kind of FDA Jobs are Available?

Due to the importance of the agency and the awe-encompassing mission at end, the FDA is constantly recruiting and looking for individuals to join their 10,000+ employee organization. FDA jobs include mission-critical medical and science positions; individuals with a background in science, engineering or medicine are strongly encouraged to research FDA jobs. In addition to applying directly through the administration’s website, the FDA attends job fairs throughout the United States to promote available positions and recruit applicants.

Currently, the FDA offers positions in the following sub departments: FDA Jobs at the Center for Biologics Evaluation and Research, FDA jobs at the Center for Drug Evaluation and Research, position at the center for Veterinary Medicine, FDA jobs at the center for Tobacco Products, jobs at the National Center for Toxicological Research and those at the Office of Science and Engineering Laboratories.

Truth About FDA Recalls

Truth About FDA RecallsWhat is the FDA?

The FDA, or the Food and Drug Administration, is a regulatory body of the United States Federal Government that is responsible for ensuring the safety of a variety of consumer products. The FDA, as a result of this expansive and critical responsibility, utilizes a plethora of resources and intelligence to exhaustively inspect various foods and drugs, which are circulated in the United States’ markets, to ensure that such items are safe, efficient, and in possession of minimal risk.

It is estimated by the FDA, that for every dollar an American citizens spends, 25 cents of that dollar will go towards the regulation and management of all products. The scope of the FDA is incredibly expansive; the administration plays a critical role in a number of industries, from pharmaceuticals to dietary supplements.

The FDA is a fundamental agency that operates within the Department of Health and Human Services. The FDA was established in 1906 under the Federal Food and Drugs Act; an act of Congress passed to appease the growing consumer concern over the safety of foods and drugs in the United States. As a result of their expansive responsibilities, the FDA is divided into a number of sub-departments.

Each department will regulate a different consumer market; there are departments within the FDA to regulate drug development, institute regulations to promote food safety, inspect the safety of cosmetics, and evaluate the effectiveness and safety of various vaccines or medical devices and research departments to evaluate the negative externalities of various consumer products. In summation, the FDA is responsible for limiting the adverse effects of basic consumer products found in the food and drug industries and for promoting the safety and effectiveness of such goods through the administration of licenses and various regulations.

What are FDA Recalls?

The Food and Drug Administration issue recalls on foods and drugs that pose threats to society. As stated earlier, the Food and Drug Administration is responsible for ensuring that the food and drug industries in America are safe and efficient; the primary tool for satisfying this mission is the recall.

FDA recalls are instituted when a product carries or distributes a significant threat to the general public. For instance, if a producer of beef distributes a mass quantity of tarnished meat, it will be recalled and thwarted from reaching the shelves at various food distributors throughout the country.

If a food is produced with a threat of salmonella, if it is reported that an outbreak is realized through the consumption of such food, the manufacturer will be forced to abide by the FDA recall laws. Additionally, if a drug is released to the market that carries a significant side effect, one that was not realized during testing trials, it will be recalled and taken out of circulation.

FDA recalls are the fundamental tool to prevent the outbreak of disease and to thwart unsafe products from reaching the shelves. Without the ability to recall food or drugs, the FDA would be powerless in limiting the negative side effects realized through unsafe or careless manufacturing efforts.

Food and Drug Administration Explained

Food and Drug Administration ExplainedWhat is the Food and Drug Administration?

The Food and Drug Administration is a Federal agency that operates within the United States Department of Health and Human Services.

The Food and Drug Administration is one of the country’s federal executive departments and is responsible for protecting and promoting public health through the supervision and regulation of tobacco products, food safety dietary supplements, prescription, as well as over-the-counter pharmaceutical drugs, biopharmaceuticals, vaccines, medical devices, electromagnetic radiation emitting devices, cosmetics, veterinary products and vaccines.

In addition to the regulation over the aforementioned products, the Food and Drug Administration enforces other laws, most notably Section 361 of the Public Health Service Act and associated legislation, which may or may not be related to food and drugs. In this format, the Food and Drug Administration is responsible for the regulation of sanitation requirements on interstate travel and the control of disease on products ranging from household pets to the donation of sperm intended for assisted reproduction.

Food and Drug Administration Quick Facts:

The following details outline the administration of the Food and Drug Administration:

The Food and Drug Administration  was formed in 1906

The headquarters of the Food and Drug Administration are located at 10903 New Hampshire Avenue in Silver Spring, Maryland. In addition to its headquarters, the Food and Drug Administration has 223 field offices and 13 laboratories located throughout the 50 states, the U.S> Virgin Islands and Puerto Rico. In 2008, the Food and Drug Administration began opening offices abroad, including in China, India, Belgium, the United Kingdom and India.

The Food and Drug Administration operates with roughly 9,500 employees and possesses an annual operating budget of 2.3 billion dollars

The Food and Drug Administration  is responsible for the jurisdiction over the Federal Government of the United States of America

The Parent Agency of the Food and Drug Administration is the Department of Health and Human Services

The head of the Food and Drug Administration is Margaret Hamburg, who acts as the Commissioner of Food and Drugs. The Commissioner of the Food and Drug Administration is appointed by the President of the United States with the direct consent of the Senate. The Commissioner reports to the Secretary of Health and Human Services.

Scope of the Food and Drug Administration:

The Food and Drug Administration regulates over $1 trillion worth of consumer goods and roughly 25% of all consumer expenditures in the United States. Total expenditures include roughly $465 billion in food sales, $275 billion in drug transactions, $60 billion in cosmetics and roughly $18 billion in dietary supplements. The majority of expenditures accounts for goods imported into the United States; the Food and Drug Administration is responsible for monitoring a third of the nation’s imports.

The majority of federal laws dealing with the Food and Administration are labeled in the Food, Drug and Cosmetics Act, which was passed in 1938 and subsequently amended, and codified in Title 21, Chapter 9 of the United States Code. 

Quick Outline of the DEA

Quick Outline of the DEA

Drug Enforcement Agency
 
 
The Drug Enforcement Agency (DEA) works under the United States Federal Government in order to keep illicit drugs off the streets, while preventing crimes which result form the manufacture and distribution of drugs. The Agency handles illicit street drugs, as well as prescription medications that have been illegally obtained.
 
 
DEA Number
 
 
A DEA number is assigned to individuals that can prescribe medications so that the DEA can then track the amount of controlled dangerous substance prescriptions are written by each doctor. If the amount or prescription seems excessive, the DEA may investigate the health care provider and their patients.
 
 
DEA Agents
 
 
DEA agents can often be identified by their uniform. However, when a DEA agent is working undercover or patrolling the streets, they may be in plain clothes. In that case, it is best to ask for a DEA badge if someone identifies themselves as a Federal agent.
 
 
DEA License
 
 
A DEA license can be used to track prescription medications around the United States. In order to prevent doctors from abusing the power to write prescriptions, the DEA will investigate a doctor when they believe the doctor is writing too many prescriptions for controlled and dangerous substances. 

Do Doctors Need DEA License

Do Doctors Need DEA License

When state and
Federal laws conflict with one another, such as the medical marijuana laws in
some states, individuals can still be prosecuted on the Federal level. This is so even
when the state would not press charges. In other words, Federal law supersedes
state law. Doctors must take part in DEA registration and obtain a DEA
license in order to prescribe certain medications. Those numbers are used to
track doctors and the prescriptions they write.

DEA registration
also prevents doctors from breaking Federal law when it conflicts with a state
law. For example, some states may allow for medical marijuana to treat some
illnesses, such as cancer and anorexia. However, medical marijuana has not been
approved by the Federal Government and it can be prosecuted as a Federal crime.
In fact, the DEA could prosecute the user, the doctor and the individual that
dispensed the prescription for the medical marijuana.

DEA registration
and a DEA license are meant to prevent the abuse of power held by doctors. They
cannot circumvent the law simply because they are doctors. In addition to
following all applicable local and state laws, they must follow Federal laws. In
fact, doctors can have their licenses revoked if they break Federal laws. They
can also have their licenses suspended if the DEA investigates them because they
suspect that they have been dispensing too many controlled dangerous substances. 

What Does A DEA Agent Do

What Does A DEA Agent Do

There are many types of DEA jobs, each of which has unique requirements and specifications. DEA agents do not necessarily deal with street crimes, as their services may be required in other areas, such as pharmacies and doctors’ offices. DEA jobs also include a variety of administrative tasks, each of which is important in preventing the manufacture and distribution of illicit street and prescription drugs.
Most employees of the DEA have a DEA badge. It is important for the public to ask for identification, such as a DEA badge, when law enforcement is plain-clothed. In fact, it is a good idea even when they are in uniform. There  has been an increase in crimes in which individuals pretend to work for law enforcement in order to commit robberies and other crimes.  
DEA agents should be easily identified by their DEA badge. However, they may be working undercover which makes them indistinguishable. In fact, many DEA jobs require that the agents be plain-clothed while they are working on the street.
DEA agents work in a variety of fields within the drug trade. They may pose undercover or simply patrol suspect pharmacies and doctors’ offices in uniform. Regardless of the job they perform, DEA jobs include individuals that are Federal employees. They have more power than state and local law enforcement and can often prosecute crimes that local law enforcement has attempted to prosecute. In fact, federal crimes are almost always prosecuted first. 

The Secrets of the DEA Number System

The Secrets of the DEA Number System

A DEA number is utilized to track individuals that write prescriptions for controlled dangerous substances. The system can be used to track physicians, as well as those that are prescribed such medications. For example, those that obtain a prescription for the same medication from two different doctors will likely be flagged in the system if the prescription is for a controlled dangerous substance.
 
 
The DEA number lookup system allows the Agency to track doctors and determine if they are prescribing a large amount of controlled dangerous substances. DEA diversion techniques, such as the controlled dangerous substance tracking systems, prevent many doctors from over-prescribing addictive and dangerous substances.
 
 
In addition, DEA diversion techniques also prevent individuals from obtaining many prescriptions for the same drugs. In the past, before the DEA number lookup system was available, individuals could more easily doctor shop and obtain many prescriptions for the same substance. Next, they would simply fill those prescriptions at different pharmacies to avoid detection. However, in order to prevent the abuse and sale of these types of drugs, the DEA number system has been put in use in more locations around the United States, not just for health care providers, but also for patients.
 
 
The DEA number system has been successful in preventing doctors from taking part in illicit activity as it relates to prescription medications. Although many prescriptions come into the country from international borders, the DEA number lookup system has prevented some of the drugs from making it to the street. 

Drug Enforcement Agency Explained

Drug Enforcement Agency Explained

The DEA, or Drug Enforcement Agency, is an agency which is supported by the United States Government. The sole purpose of the DEA is to prevent the manufacture, sale and distribution of illicit drugs. In addition, the DEA enforces the laws which govern prescription medications and can criminally charge individuals that have possession of prescription medication that does not belong to them. Often, the penalties for having an unauthorized prescription is similar to that utilized for illicit street drugs.
Working under the United States Department of Justice, the DEA is the primary agency in charge of drug enforcement management. They are responsible for enforcing the Controlled Dangerous Substance Act and often work in concert with the Federal Bureau of Investigaton (FBI).
In general, drug enforcement agents are the sole individuals that may pursue drug cases across the United States borders. For example, they may look for known drug traffickers abroad when they have the cooperation of the other country’s government.
The creation of the DEA took place under President Nixon, who sought to have a single agency be in charge of preventing drug crimes in the United States. The DEA was meant to enforce the Federal drug laws across the country, even when they conflicted with state laws. In addition, the DEA was charged with drug control and the prevention of drug-related crimes. 
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