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Accredited Drug Testing provides a wide range of drug and alcohol testing services across 35 centers in the Irvine, California area. We conduct DOT and non-DOT urine screenings, breath alcohol analyses, EtG alcohol tests, and hair drug testing suitable for personal, corporate, and legal purposes. Our facilities in Irvine, CA offer quick-result testing and SAMSA accredited lab assessments, with same-day services available. Most testing sites are conveniently located close to homes or offices. Additional services encompass Occupational Health Testing, Clinical Testing, and Background Checks.
Contact us at (800) 221-4291 or register via our website. Just choose your test and pick a nearby center for testing—suitable for personal, employee, or third-party needs. Scheduling is quick and convenient; reach our scheduling team or arrange your test online anytime. Our efficient and easy-to-navigate process enables you to set up drug testing in Irvine 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 Irvine 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, Irvine in Orange County reported 150 drug-related arrests.
The county saw a 10% increase in opioid overdoses in 2021.
Irvine, Orange County, ranked fifth in the county for drug treatment admissions in 2022.
Irvine had a 15% increase in methamphetamine seizures in 2021.
48% of drug crime arrests in Irvine involved young adults aged 18-25 in 2022.
Orange County health officials recorded 300 hospitalizations related to substance abuse in Irvine in 2021.
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 Irvine, CA, employers play a crucial role in maintaining a drug-free workplace. Many organizations implement drug testing policies as part of their hiring process and regular employee evaluations. This approach helps identify and provide support to employees battling substance abuse.
Resources such as the California Department of Industrial Relations offer guidance and policies to ensure compliance. Employers partner with local health services to facilitate treatment and counseling, adhering to standard state regulations in their drug testing protocols.
In Irvine, CA, government efforts to address drug problems involve collaboration with state and federal agencies. The Orange County Health Care Agency provides resources for prevention and treatment. Additionally, Irvine aligns with the California Department of Health Care Services for statewide initiatives.
The Irvine Police Department actively participates in drug education and enforcement programs. They collaborate with local schools and communities to foster a safer environment. Enhanced support systems, like counseling and referral services, are integral to their strategy to deter drug abuse.
Irvine, CA, has witnessed several significant local drug busts, underscoring the ongoing battle against substance trafficking. In 2022, the Irvine Police Department reported a major interception of a methamphetamine shipment, resulting in multiple arrests.
Community outreach programs have been pivotal in these efforts. The annual drug awareness week in Irvine educates residents on the dangers of drug abuse and features panel discussions with law enforcement and healthcare professionals. This has been instrumental in reducing local demand and trafficking.
Accredited Drug Testing offers fast, reliable employment screening services in Irvine, CA. Trusted by employers nationwide for accurate results and exceptional service.
California DOT/Non DOT Physicals
Alcohol and Drug Program Administration
California Access to Recovery
California Association of Addiction Hospitals
Partnership for Drug-Free Kids
SAMHSA
Orange County Alcohol and Drug Abuse Services
Forward Choices
Robert's Center
Salvation Army Substance Abuse Programs
The Orange County Recovery Center
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Quickly find a local DOT drug testing center in Irvine, CA — fast, reliable, convenient nationwide service!
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This is by far the easiest way to get my lab work ordered and paid for. The phone calls are short and to the point. They don’t try to push extra sales on you and when I walk in to the clinic I simply show my donor pass and with in a matter of minutes I’m done. I will continue to use ADT in the future.
Jason Jackson - 7/19/2025
Everything was great, the staff was very polite. Thank you.
Olga Petrova - 9/19/2024
The visit here is always the best . The place is always really clean. The employees are super courteous, very polite, and professional. This is the only drug lab I like to go do my drug and alcohol test. I would like to tell them thank you so much for thier excellent performance and job
Eli Gonzalez - 1/4/2025