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Our accredited drug testing services cover a wide array of screenings, conveniently available at 35 testing facilities around Standish, Maine. Whether you need DOT or non-DOT urine tests, breath alcohol assessments, EtG alcohol checks, or hair drug tests, we cater to individual, corporate, and legal requirements. Rapid testing and SAMSA-certified lab analysis are offered in Standish, ME, with same-day services available. Most centers are just a short distance from local residences or workplaces. Additional offerings include Occupational Health Testing, Clinical Testing, and Background Verification.
To schedule a test, dial (800) 221-4291 or use our online portal. Choose your test, select a convenient site, and arrange the service for yourself, your staff, or others with ease. Our straightforward and accessible system ensures you can set up testing near Standish seamlessly, any time. Whether you call our team or book digitally, organizing your test is always fast 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 Standish 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 Standish, ME, located in Cumberland County, opioid-related deaths significantly increased by 15% from 2020 to 2021.
The town of Standish reported a 12% rise in drug-related arrests in 2022 compared to the previous year.
Cumberland County, home to Standish, saw a 25% increase in emergency room visits due to drug overdoses in 2021.
A survey in Standish, ME revealed that nearly 8% of high school students had tried drugs before age 13 in 2021.
In 2022, Standish, ME, reported a 10% increase in admissions to drug rehabilitation centers compared to 2020.
Standish, ME accounted for approximately 2% of all opioid-related health incidents recorded in Cumberland County 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
Employers in Standish, ME, adopt strict drug testing policies, ensuring a safe workplace. Given the rise in drug-related incidents, there is an emphasis on pre-employment screening and random drug tests as per industry standards. Local businesses often collaborate with the Occupational Safety and Health Administration for guidelines on maintaining drug-free workplaces.
Moreover, the Maine Department of Labor guides employers on implementing comprehensive drug policies, aiming to provide support rather than only punitive measures. Many employers offer programs for employee assistance, such as confidential counseling services, to help those struggling with addiction.
The government of Standish, ME, alongside Cumberland County, has been proactive in tackling the drug crisis. Efforts include partnerships with the Office of Behavioral Health to provide treatment resources, focusing on harm reduction and rehabilitation.
Additionally, the Maine State Government, through initiatives like the Maine Drug Enforcement Agency, is intensifying crackdowns on drug distribution networks. Community programs focusing on education and awareness, supported by the town council, aim to reduce drug initiation among youths.
In Standish, ME, local authorities recently conducted a significant drug bust, uncovering a smuggling operation intersecting with nearby towns. The operation led to multiple arrests and seizure of illegal substances. Collaboration between the local police department and state agencies was crucial in efficiently dismantling this network.
The community in Standish has been increasingly concerned about the impact of drug trafficking. Awareness campaigns and community meetings have been organized to discuss preventive measures and support systems for those affected. These efforts aim to strengthen relations between law enforcement and residents and reduce drug-related incidents.
Standish law enforcement has also reported an uptick in the use of illegal substances among youth, prompting local schools to introduce educational programs. These initiatives focus on the dangers of drug use and provide students with resources and support to make safe choices. Community leaders are hopeful these efforts will contribute to long-term positive changes.
Accredited Drug Testing offers fast, reliable employment screening services in Standish, ME. Trusted by employers nationwide for accurate results and exceptional service.
Maine Prevention Store
Substance Abuse and Mental Health Services
Maine Drug Rehab
Portland Recovery Community Center
Healthcare.gov
Office of Behavioral Health
Maine CDC
Bethesda Maine Memorial
Northeast Addiction Consultants
Dirigo Counseling Clinic
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Time was running out before my Cdl got downgraded because of a violation I had on clearinghouse. I couldn't find an employer to send me for my return to duty test, but these guys had my test scheduled and done in the same day! They saved my cdl. Thank you again!
Michael Williams - 12/2/2024
I always have a good experience setting up company driver drug screens through ADT. I'm really happy I found them while searching online, they have made my job much easier.
Exodus Heath - 2/13/2025
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