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Accredited Drug Testing provides a full range of drug and alcohol tests at 40 locations in and around Readington, NJ. Our services include DOT and non-DOT urine drug exams, breathalyzer tests, EtG alcohol assessment, and hair follicle tests for individuals, workforce, and legal requirements. Conveniently situated near homes and offices in Readington, these centers offer quick turnaround tests and SAMSA certified lab evaluations—most results can be expedited with our same-day services. We also conduct Occupational Health Testing, Clinical Assessments, and Background Screenings.
Dial (800) 221-4291 or opt for online registration. After selecting a test, choose a nearby center—testing solutions are available for personal, employee, or third-party use. Our straightforward scheduling system enables rapid test arrangements, either through our dedicated team or via our 24/7 online platform. This efficient and intuitive process makes arranging testing in Readington simple.
* You must register by phone or online to receive your donor pass/registration prior to proceeding to the testing center. You must bring a valid government issued ID along with the registration/barcode number which was sent to you by email.
When you're searching for drug testing near me or drug testing locations, we provide a simple and convenient process to find a drug and alcohol testing location near you that is certified to provide all of your drug and alcohol testing needs.
At our Readington drug testing collection sites, Accredited Drug Testing provides one of the widest selections of drug and alcohol testing services available. Whether you're an employer, attorney, court, or private individual, we offer both DOT and non-DOT testing options—ranging from rapid tests to comprehensive lab-based screenings—capable of detecting nearly any substance.
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If you're an employer needing to test 25 or more employees and looking to save time and money, we offer mobile on-site drug testing where we come to you. Call us today for more information.
In Readington, NJ, Hunterdon County, 8% of high school students reported using illegal drugs in the past year.
Readington Township, NJ, Hunterdon County, reported 15 opioid-related overdoses in the last reported year.
Hunterdon County, which includes Readington, NJ, saw a 5% increase in drug-related arrests over the past year.
In Readington Township, NJ, drug abuse is most prevalent among individuals aged 18-25.
37% of drug-related offenses in Readington, NJ, involved prescription drug abuse, according to recent data.
Readington, NJ, in Hunterdon County recorded a 12% increase in drug rehabilitation admissions.
Drug elimination is the sum of the processes of removing an administered drug from the body. In the pharmacokinetic ADME scheme (absorption, distribution, metabolism, and excretion), it is frequently considered to encompass both metabolism and excretion. Hydrophobic drugs, to be excreted, must undergo metabolic modification making them more polar. Hydrophilic drugs, on the other hand, can undergo excretion directly, without the need for metabolic changes to their molecular structures.
Although many sites of metabolism and excretion exist, the chief organ of metabolism is the liver, while the organ primarily tasked with excretion is the kidney. Any significant dysfunction in either organ can result in the accumulation of the drug or its metabolites in toxic concentrations.
A variety of other factors impact elimination — intrinsic drug properties, such as polarity, size, or pKa. Also other factors include genetic variation among individuals, disease states affecting other organs, and pathways involved in the way the drug distributes through the body, such as first-pass metabolism.
Drug elimination is the removal of an administered drug from the body. It is accomplished in two ways, either by excretion of an unmetabolized drug in its intact form or by metabolic biotransformation followed by excretion. While excretion is primarily carried out by the kidneys, other organ systems are involved as well. Similarly, the liver is the primary site of biotransformation, yet extrahepatic metabolism takes place in a variety of organ systems affecting multiple drugs.
Given the multiple organ systems and the variety of metabolic transformations present, drug elimination can entail a significant degree of complexity. Hydrophilic drugs are typically directly excreted by the kidneys, while hydrophobic drugs undergo biotransformation before excretion. The purpose here is twofold – biotransformation serves both detoxify the exogenous substances as well as to increase their hydrophilicity, ensuring their elimination via the kidneys.
Two broad metabolic pathways of hepatic drug transformation exist. Phase I is the direct modification of the target molecule, whereas phase II entails conjugation of the target to a polar molecule of low molecular weight. Phase I prepare the drug to enter phase II, but single-phase metabolism also exists.
Phase I involves oxidation, reduction, and hydrolysis of the exogenous molecule. These reactions are accomplished by hepatic microsomal enzymes, which reside in the smooth endoplasmic reticulum of the hepatocytes. Best known among them is the cytochrome P450 system, whose enzymes are predominantly involved in oxidative metabolism. Within the cytochrome P450 family (CYP), the enzyme responsible for the metabolism of more than 50% of existing drugs is the CYP3A4. Its activity encompasses various classes of medications, including opioids, immunosuppressants, antihistamines, and benzodiazepines. The enzymes can also be induced or inhibited by a variety of substances they interact with, including pharmaceuticals. The increase in metabolic activity with CYP induction results in a diminished activity of drugs targeted by that particular isoform. Conversely, CYP inhibition will result in increased drug plasma concentration, potentially leading toxicity. The CYP3A4 is induced by phenytoin, phenobarbital, and St. John's wort, while diltiazem, erythromycin, and grapefruit inhibit it. Caution is, therefore, necessary when administering CYP3A4-metabolized drugs in the presence of any of the inhibitors or inducers.
Phase II consists of covalent bonding of polar groups to nonpolar molecules to render them water-soluble and allow renal or biliary excretion. Target molecules enter phase II directly or via initial processing through phase I. A variety of polar adjuncts is transferred, including amino acids, glucuronic acid, glutathione, acetate, and sulfate. Glucuronidation is one of the major pathways of phase II biotransformation. The UDP-glucuronosyltransferase (UGT) enzyme family performs this activity. Typically, glucuronide derivatives possess less or no activity of the original drug, but in some cases, pharmacologically active compounds result. Morphine-6-glucuronide is a phase II metabolite of morphine with significant analgesic activity. As with the CYP enzymes, inducers, and inhibitors of phase II, enzymes exist and may influence the efficacy of drugs that rely on conjugation before excretion.
The first-pass effect is a feature of hepatic metabolism that also plays a role in the elimination of multiple drugs. Here, the enteric consumed drugs are exposed directly to the liver via the portal vein, where they undergo biotransformation before entering the systemic circulation. This activity reduces the bioavailability and needs to be factored into the dose administered to the patient. Intravenously administered drugs are not subject to the first-pass effect.
Extrahepatic drug metabolism takes place in the GI tract, kidneys, lungs, plasma, and skin.
Renal excretion completes the process of elimination that begins in the liver. Polar drugs or their metabolites get filtered in the kidneys and typically do not undergo reabsorption. They subsequently get excreted in the urine. Urinary pH has a significant impact on excretion, as drug ionization changes depending on the alkaline or acidic environment. Increased excretion occurs with weakly acidic drugs in basic urine and weakly basic drugs in acidic urine.
Excretion in the bile is another significant form of drug elimination. The liver can actively secrete ionized drugs with a molecular weight greater than 300 g/mol into bile, from where they reach the digestive tract and are either eliminated in feces or reabsorbed as part of the enterohepatic cycle.
Other pathways of excretion include the lungs, breast milk, sweat, saliva, and tears
Employers in Readington, NJ, Hunterdon County, are increasingly adopting stringent drug testing policies to maintain a safe work environment. Many companies require pre-employment drug screenings and may conduct random tests to ensure compliance and safety at the workplace.
The New Jersey Department of Labor provides guidelines that help Readington employers create drug-free workplace policies. These include provisions for counseling and support services for employees struggling with addiction.
Local companies often collaborate with the Substance Abuse and Mental Health Services Administration (SAMHSA) to design programs that proactively tackle workplace substance abuse, ensuring both support and responsibility among employees.
The government of Readington, NJ, in Hunterdon County, has implemented several strategies to address drug issues. Local task forces have been enhanced to improve coordination between law enforcement and community services. Programs aimed at prevention and education are sponsored by the Readington Township Department of Health.
Efforts are also made at the state level through New Jersey's Office of the Attorney General, which supports community-based prevention initiatives. The state provides resources and funding to local agencies focused on reducing drug abuse and enhancing public awareness.
Recent drug-related events in Readington, NJ, Hunterdon County, included a significant drug bust that led to multiple arrests and seizures of illegal substances. In a coordinated operation, local law enforcement dismantled a drug distribution ring that was active in the area.
In addition to law enforcement activities, Readington also hosts community events aimed at increasing awareness about drug abuse. These events foster open conversations about addiction and recovery, and often involve local organizations and experts sharing insights on tackling these issues.
The Readington Police Department works closely with neighboring towns in Hunterdon County for regular drug awareness campaigns, focusing on educating young adults about prevention and available support systems.
Accredited Drug Testing offers fast, reliable employment screening services in Readington, NJ. Trusted by employers nationwide for accurate results and exceptional service.
New Jersey DOT/Non DOT Physicals
New Jersey Department of Human Services
Hunterdon County Substance Abuse Resources
New Jersey Attorney General's Office Drug Initiatives
NJ 211 Drug Addiction Resources
Hunterdon Healthcare Drug Rehabilitation
Substance Abuse and Mental Health Services Administration (SAMHSA)
Department of Homeland Security Drug Awareness
Recovery Centers of America
U.S. Attorney’s Office, District of New Jersey
NJ CARES Data Dashboard
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Trish last week and Tatiana this week, very fun and easy folks to deal with. Well be using them more and more in the future.
Tom O - 12/19/2024
Trish was amazing and got me through the sytem very fast and swift. I had a hard time hearing her a couple of times, but she was super sweet and helpful throughout the process. Highly recommend her!
Sophia Schutze - 6/19/2024
I've had to use this service twice for out of state physicians we've hired and both times it was super easy. Both customer service reps I spoke with were super helpful and courteous. I won't hesitate to use their service again if needed.
Alicia Rau - 6/19/2024