Our automated scheduling system is available 24/7. Order your test online and receive your donor/registration pass by email. Click Here
Same Day Service
Accredited Drug Testing provides extensive drug and alcohol assessments at our 29 locations in the Cloverdale, Alabama vicinity. Our services include both DOT and non-DOT urine testing, breath alcohol assessments, EtG alcohol analyses, and hair drug examinations designed for personal, corporate, and legal requirements. In the Cloverdale area, results are available quickly, and our labs are SAMSA certified. Many testing centers are conveniently situated, just a short distance from homes or offices, offering same-day service. We also conduct Occupational Health Testing, Clinical Evaluations, and Background Screening.
Dial (800) 221-4291 or sign up online. Choose your desired test and a convenient location nearby—testing caters to self, employees, or third parties. Executing test arrangements is swift and straightforward; contact our scheduling team or arrange your test online, accessible 24/7. Our efficient and user-friendly system simplifies organizing your drug test near Cloverdale with ease.
* 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 Cloverdale 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 2022, Cloverdale, Lauderdale County reported a 45% increase in opioid-related incidents.
Lauderdale County saw a 35% rise in methamphetamine-related arrests in 2021.
Cloverdale's drug overdose death rate increased by 20% between 2020 and 2022.
Alabama Department of Public Health noted a spike in heroin use cases in Cloverdale in 2023.
In 2021, Cloverdale documented over 200 drug abuse rehabilitation admissions.
Lauderdale County law enforcement reported over 300 drug-related offenses in Cloverdale in 2022.
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 Cloverdale, AL, are increasingly implementing strict drug testing policies. Companies often partner with organizations like the U.S. Department of Labor to ensure compliance with workplace regulations.
Several local businesses require pre-employment and random drug testing to maintain a safe work environment, contributing to the wider community effort against substance abuse.
The government in Cloverdale, AL has initiated several programs to combat drug issues. The Lauderdale County Drug Task Force works closely with local authorities to address substance abuse concerns through targeted operations and community outreach.
The state of Alabama also contributes via agencies like the Alabama Department of Economic and Community Affairs, which offers funding and resources for drug prevention programs.
Cloverdale, AL has witnessed several significant drug busts, highlighting ongoing law enforcement efforts. For instance, in early 2023, a major operation led to the confiscation of large quantities of illegal substances and multiple arrests.
Community events aimed at raising awareness and reducing stigma associated with drug abuse are also common, leading to increased public participation and support for rehabilitation services.
Accredited Drug Testing offers fast, reliable employment screening services in Cloverdale, AL. Trusted by employers nationwide for accurate results and exceptional service.
Alabama Department of Mental Health
Bradford Health Services
Recovery Place
The Council on Recovery
Fitzgerald Recovery Center
Lawrence Co. Addiction Center
Wellstone Behavioral Health
AIDS Action Coalition
Birmingham Crisis Center
SpectraCare Health Systems
Quickly find trusted local drug testing centers in Cloverdale, AL — fast, convenient, and reliable every time!
Quickly find a local DOT drug testing center in Cloverdale, AL — fast, reliable, convenient nationwide service!
DNA testing for legal and non-legal purposes including child support, and child custody around Cloverdale, AL.
Including specimen collector training, DER training, reasonable suspicion training and much more in Cloverdale, AL.v
Get fast, accurate hair drug testing at our convenient Cloverdale, AL locations—results you can trust, every time!
Fast, reliable alcohol testing to keep your workplace safe and compliant every single day in Cloverdale, AL.
Reliable nationwide drug testing services ensuring accuracy, compliance, and quick results for businesses and individuals in Cloverdale, AL.
Accurate 5 panel drug testing with fast, confidential results—trusted by Cloverdale, AL employers and individuals nationwide.
Comprehensive 10 panel drug testing with fast, reliable results—trusted for Cloverdale, AL workplace and personal testing needs.
Convenient on-site mobile drug testing with fast, reliable results—saving time while keeping your Cloverdale, AL workplace compliant.
Certified DOT physicals with quick, reliable exams to keep Cloverdale, AL drivers compliant and on the road with confidence.
Join our DOT consortium for hassle-free compliance, random testing management, and reliable driver safety solutions.
Torin was great. Explained everything so no questions
Tony Lombardo - 4/18/2025
Very easy to get scheduled and easy process once checked in and the staff were all extremely friendly! I would recommend this company!
Ronickia Moore - 11/19/2024
I use their service for new hire and DOT employee's. Spoke with Taisha Walker this morning, and she was very helpful. She made the process smooth and seamless.
Christina Galdos - 3/9/2025