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Accredited Drug Testing provides all-inclusive drug and alcohol testing services at our 40 testing locations in the Cross Keys, New Jersey area. Our offerings include DOT, non-DOT urine tests, breath alcohol, EtG alcohol analysis, and hair drug testing tailored for personal, business, and legal requirements. In Cross Keys, NJ, we deliver quick result tests and analyses certified by SAMSA laboratories. With same-day services available, most testing centers are conveniently close to your home or workplace. We also offer Occupational Health Testing, Clinical Testing, and Background Checks.
Dial (800) 221-4291 or use our online registration. Choose your test and select a nearby facility—testing can be scheduled for yourself, an employee, or another individual. Scheduling is Fast and Easy; reach our scheduling department or book your test online at any time. Our efficient and streamlined process facilitates easy drug testing arrangements near Cross Keys.
* 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 Cross Keys 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.
DOT Drug Testing and Requirements
DOT Employer Drug Policy Development
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 Cross Keys, NJ, Gloucester County, opioid-related overdose deaths totaled 61 in the latest report.
Gloucester County, where Cross Keys is located, reported 1,043 naloxone administrations in one year.
Cross Keys, NJ sees 3.2% of its residents seeking treatment for substance abuse disorders.
Alcohol remains the primary substance of abuse with 45% reported cases in Gloucester County.
Marijuana abuse in Gloucester County accounts for 20% of substance-related treatments.
Cross Keys, NJ has witnessed a 15% increase in drug-related crime over two years within Gloucester County.
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 Cross Keys, NJ, are cognizant of the significance of maintaining a drug-free workplace as a means to ensure safety and productivity. Many local businesses adhere to the New Jersey Drug-Free Workplace laws, enforcing policies that include varied drug testing methods. The DEA's Newark Division provides guidance on implementing effective workplace drug policies.
Local employers frequently participate in state-run training sessions, which are facilitated by the New Jersey Department of Labor and Workforce Development. These sessions aim to educate employers on best practices for drug testing and for creating a supportive environment for employees grappling with substance use issues. Consequently, companies emphasize the importance of balancing between enforcing policies and supporting employee rehabilitation efforts.
The government in Cross Keys, NJ, is committed to combating drug-related problems through various initiatives and partnerships. Gloucester County's coalition with the Addiction Recovery Task Force emphasizes community awareness and preventive measures. These efforts are focused on providing educational programs for all ages, promoting awareness of the dangers of drug abuse, and fostering robust community support systems.
Furthermore, programs like the Medication-Assisted Treatment Initiative provide essential support for those struggling with addiction throughout New Jersey, including Cross Keys. Additionally, federal support via the Substance Abuse and Mental Health Services Administration (SAMHSA) aims to ensure comprehensive coverage of addiction treatment, with financial and logistical backing for state-level efforts.
Cross Keys, NJ, witnessed a significant drug bust in 2022 when local authorities collaborated with the Gloucester County Prosecutor's Office to dismantle a significant narcotics distribution network. The operation led to multiple arrests and the seizure of substantial quantities of illicit substances.
Another noteworthy event was the comprehensive community outreach program spearheaded by the New Jersey State Police in Cross Keys. This initiative involved anonymous tip lines and community workshops aimed at fostering cooperation between residents and law enforcement to tackle drug-related crimes effectively.
Accredited Drug Testing offers fast, reliable employment screening services in Cross Keys, NJ. Trusted by employers nationwide for accurate results and exceptional service.
New Jersey DOT/Non DOT Physicals
New Jersey Division of Mental Health and Addiction Services
Recovery.org
SAMHSA National Helpline
NJ Counties Addiction Recovery Resources
Gloucester County Addiction Recovery Task Force
National Institute on Drug Abuse (NIDA)
Partnership for Maternal and Child Health of Northern New Jersey
Caron Treatment Centers - Charleston
Drug-Free NJ Hotlines
RehabInfo
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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