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At our 30 testing centers across the Red Springs, NC area, Accredited Drug Testing delivers extensive drug and alcohol testing services. We conduct both DOT and non-DOT urine tests, breath alcohol exams, EtG alcohol evaluations, and hair drug assessments for personal, corporate, and legal needs. In Red Springs, NC, we ensure rapid test results and offer SAMSA certified lab analysis, with same day options available. Most testing centers in Red Springs are conveniently located near your residence or office. We also provide Occupational Health Testing, Clinical Testing, and Background Check services.
Reach us at (800) 221-4291 or register online. Easily choose the type of test and a nearby location—services are available for personal, employee, or third-party testing. With our seamless process, book your test quickly via our scheduling team or online, anytime. Experience a hassle-free way to set up drug testing near Red Springs.
* 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 Red Springs 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 2021, Red Springs, located in Robeson County, NC, reported a drug-related crime rate increase of 15% from the previous year.
Red Springs, Robeson County, ranked among the top 10% in NC for opioid overdose deaths in 2020.
Youth drug abuse in Red Springs, Robeson County, NC is reportedly rising, with 12% of high school students having tried illicit drugs (2022 survey).
Robeson County, including Red Springs, recorded over 50 drug trafficking cases in 2022.
In Red Springs, NC, the drug abuse treatment admissions have doubled since 2018, according to Robeson County health reports.
Robeson County, encompassing Red Springs, saw a 30% increase in methamphetamine use in 2021 compared to 2019.
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 Red Springs, NC, have recognized the impact of drug abuse on workplace safety and productivity. Many businesses now implement stringent drug testing policies as part of their hiring and employment process. Random drug testing is not uncommon, reflecting a commitment to a drug-free work environment. The goal is to deter substance abuse and ensure the well-being of employees and the public. Employers adhere to guidelines provided by the North Carolina Department of Commerce, ensuring compliance with state regulations.
Moreover, companies actively participate in awareness campaigns and workshops conducted in coordination with local health departments. Emphasis is placed on support structures, such as employee assistance programs, to help rehabilitate those struggling with addiction.
The government in Red Springs, NC, alongside Robeson County officials, has launched several initiatives to address the drug problems plaguing the area. These efforts include enhanced support for local law enforcement and increased community outreach concerning substance abuse. In collaboration with state agencies, Robeson County has focused on educational programs aimed at prevention and recovery support. Furthermore, partnerships have been formed with organizations like the North Carolina Department of Health and Human Services to extend resources and services to affected individuals.
Recent law enforcement actions in Red Springs, NC, have successfully led to several significant drug busts. For instance, a high-profile operation last year resulted in the confiscation of large quantities of illegal substances, significantly reducing drug availability in the area. The coordinated effort between local police and federal agencies underscores the ongoing commitment to combating illegal drug distribution. These operations often involve undercover investigations and tips from community members, reflecting the community's involvement in addressing the endemic problem.
Such events not only curb the immediate drug supply but also send a strong message deterring future illegal activities. Continuing this aggressive approach, authorities are collaborating with neighboring regions to dismantle networks operating beyond local boundaries, transforming Red Springs' narrative
Accredited Drug Testing offers fast, reliable employment screening services in Red Springs, NC. Trusted by employers nationwide for accurate results and exceptional service.
North Carolina DOT/Non DOT Physicals
North Carolina Department of Health and Human Services
North Carolina o-drug Settlement
North Carolina Department of Cultural Resources
North Carolina Department of Justice
North Carolina Medical Board
NC Health Info
Robeson County Health Department
Alcohol & Drug Council of North Carolina
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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