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Accredited Drug Testing delivers wide-ranging drug and alcohol assessment solutions through our 29 testing centers situated in Dobson, North Carolina. Our array of services comprises DOT and non-DOT urine analyses, breath alcohol evaluations, EtG alcohol assessments, and hair follicle examinations, suited for individuals, businesses, and legal entities. In Dobson, NC, we facilitate rapid response testing and SAMSA-certified laboratory evaluations, with same-day service on offer, ensuring most testing facilities are just a short distance from your residence or workplace. We also provide Occupational Health Assessments, Clinical Tests, and Background Verification services.
To schedule, dial (800) 221-4291 or register online. Choose your desired test and the nearest venue—services are available for yourself, employees, or others. Scheduling is swift and intuitive; contact our scheduling team or arrange your testing online any time. Our efficient process makes organizing a drug test near Dobson seamless and straightforward.
* 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 Dobson 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 2020, Dobson, NC, located in Surry County, reported a 15% increase in opioid-related emergency room visits.
Surry County recorded 30 drug overdose deaths in 2019, with Dobson contributing significantly to this statistic.
The 2021 Surry County Health Report noted a 12% rise in substance abuse treatment admissions from Dobson, NC.
In 2019, nearly 60% of drug arrests in Surry County were from Dobson, highlighting rising substance abuse issues.
Surry County's 2020 Substance Use Survey indicated that 1 in 4 high school students in Dobson had tried an illicit drug.
A 2021 study showed that Dobson accounted for 35% of Surry County's opioid prescription rates, underscoring local abuse concerns.
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 Dobson, NC, have adopted stringent drug testing policies to ensure a safe and drug-free workplace. Most companies conduct pre-employment and random drug testing to deter substance abuse among employees. This is in line with North Carolina's emphasis on maintaining a healthy workforce, aligning local policies with state and federal employment standards. The North Carolina Department of Labor website outlines these workplace policy requirements to support employers in implementing effective drug testing measures.
The government of Dobson, NC, which lies in Surry County, has been actively pursuing solutions to its drug problems. Various programs are in place, focusing on prevention and intervention. Surry County's Health and Nutrition Center website provides resources for those seeking help. Additionally, Dobson collaborates with state agencies such as the North Carolina Department of Health and Human Services NCDHHS. This partnership aims to reduce opioid prescriptions, increase addiction treatment access, and educate the public on drug use awareness through comprehensive community outreach initiatives.
In recent years, Dobson, located in Surry County, has seen several high-profile drug busts aimed at curbing the local drug trade. Collaborations between local law enforcement and federal agencies have led to significant seizures, including a major operation in early 2023 that resulted in multiple arrests and the confiscation of illegal substances. These actions, according to reports in the local news, have been part of a strategic enforcement plan to disrupt drug networks in the region. Community events such as drug education seminars and involvement in national drug take-back initiatives are also part of Dobson's efforts to combat substance abuse and its effects on the community.
Accredited Drug Testing offers fast, reliable employment screening services in Dobson, NC. Trusted by employers nationwide for accurate results and exceptional service.
North Carolina DOT/Non DOT Physicals
Surry County Health and Nutrition Center
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North Carolina Health News
Drug Rehab NC
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Charlotte Crime Watch
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NIH Drug Abuse Stats
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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