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At Accredited Drug Testing, we offer a wide range of drug and alcohol testing services at our 38 locations near Bloomingdale, New Jersey. Our offerings include DOT-compliant and standard urine screens, breathalyzer exams, EtG alcohol assessments, and hair follicle testing for personal, professional, and legal purposes. We guarantee quick result processing and utilize SAMSA-certified labs. Conveniently located, many Bloomingdale testing facilities are only a short distance from your workplace or residence. Additional offerings cover Occupational Health, Clinical Assessments, and Background Screenings.
For scheduling, dial (800) 221-4291 or simply register online. Choose the test you need and select a nearby center—available for personal, workforce, or third-party testing. Scheduling is quick and seamless, whether you call our dedicated team or use our round-the-clock online system. Our efficient and accessible booking process enables easy arrangement of drug testing in Bloomingdale.
* 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 Bloomingdale 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 Bloomingdale, NJ, Passaic County, opioid-related deaths increased by 15% from 2020 to 2021.
Passaic County reported that 10% of high school students in Bloomingdale admitted to experimenting with illicit drugs.
In 2022, Bloomingdale saw a 5% rise in admissions to rehabilitation centers for drug abuse issues.
The emergency room visits in Passaic County for drug overdoses rose by 12% between 2019 and 2021.
Passaic County reported 120 drug arrests in Bloomingdale in a recent year, reflecting an increase compared to prior years.
Bloomingdale, NJ, documented a significant increase in methamphetamine use in the younger population in 2020.
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
In Bloomingdale, NJ, employers are increasingly implementing rigorous drug testing policies to ensure a safe workplace. Many local companies insist on pre-employment drug screening and random testing to maintain safety and productivity. These policies adhere to state regulations set by the New Jersey Department of Labor and Workforce Development.
Organizations in Bloomingdale are also providing support for employees struggling with substance abuse, offering access to Employee Assistance Programs (EAPs). This initiative helps workers access necessary rehabilitation and counseling services to foster recovery and well-being.
As drug abuse remains a concern, Bloomingdale employers collaborate with external agencies to stay compliant with federal guidelines and adapt to evolving workplace safety needs. The proactive approach ensures a harmonious and effective working environment.
The government of Bloomingdale, NJ, in collaboration with Passaic County authorities, has initiated several programs to tackle drug abuse. These include public awareness campaigns and increased funding for local rehabilitation centers. NJ Department of Health and NJ Office of the Attorney General work together to support these efforts.
Community-based initiatives, supported by grants from the Substance Abuse and Mental Health Services Administration (SAMHSA), aim to reduce substance abuse through education and outreach. The involvement of local schools and non-profits has been crucial in fostering a safer environment for the residents of Bloomingdale.
In recent news, local law enforcement agencies in Bloomingdale, NJ, have conducted a successful drug bust targeting a key distribution ring within the area. This operation was the culmination of months of investigative work and led to multiple arrests along with the confiscation of substantial quantities of illicit substances, believed to be opioids and amphetamines.
The Bloomingdale Police Department recently reported a significant decrease in drug-related incidents, attributed to the continuing collaborative efforts with regional task forces. These combined resources have enhanced patrol strategies and surveillance capabilities, focusing on disrupting known hotspots for drug activity.
Community outreach programs have been emphasized in the area following drug busts, as Bloomingdale aims to address the root causes of substance abuse. Initiatives aimed at providing education and support to residents affected by drug-related issues are underway, fostering a collaborative approach to a safer community.
Accredited Drug Testing offers fast, reliable employment screening services in Bloomingdale, NJ. Trusted by employers nationwide for accurate results and exceptional service.
New Jersey DOT/Non DOT Physicals
NJ 211 Substance Abuse Treatment Resources
Center for Drug Addiction
Oak Hill Center
New Jersey Drug Abuse Resources
NJ Health Drug Abuse
Prevention Links
Gateway Foundation New Jersey
Recovery.org New Jersey
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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