From HR Dive: "Although the positive drug test rate dropped slightly for safety-sensitive roles, workers in these roles also had a marked increase in cheating attempts, Quest Diagnostics found."
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According to an analysis by Quest Diagnostics of 9.8 million anonymized workforce drug tests, the positive drug test rate slightly decreased for safety-sensitive roles. Still, there was a noticeable increase in cheating attempts among workers in these positions. Unlike urine tests, fingerprint drug testing is a non-invasive, hygienic, and tamper-proof solution to drug test cheating. It collects sweat from a fingerprint, making substitution or adulteration almost impossible. Additionally, it provides immediate results and enhances detection accuracy, ensuring timely and relevant screenings. https://bit.ly/3ztMCPd #drugtest #workplacesafety #whs
Drug test cheating soared last year
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Today's WSJ article sheds light on the potential shortcomings of traditional workplace drug testing methods. Our innovative sweat testing methodology stands out as a proven, simple, and rapid solution. It offers unparalleled accuracy and reliability, setting a new standard for workplace safety and integrity. Leaders who ignore the pitfalls of existing technology can no longer hide behind ignorance; it’s time to embrace superior solutions.
Workers cheating on drug tests have reached the highest rate in over 30 years*, posing serious safety risks in the workplace. Quest Diagnostics reports a sixfold increase in substituted urine samples, highlighting the urgent need for solutions that ensure sample integrity and reduce tampering. https://lnkd.in/dvNiBCF2 * Quest Diagnostics
More Workers Are Cheating on Drug Tests
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beechtreediagnostics.com [email protected] 4I5-424-8247 Want to try something new? Is your existing provider not doing very well? Give me a call. I am open to do a presentation. The services we provide will benefit you and your team Urine toxicology testing is an important tool in evidence-based patient care. The types of clinical situations in which clinical drug testing can be used includes pain management with opioid medications, office-based opioid treatment, behavioral health when prescribing medications, such as anti-depressant therapy, and other situations when risk for substance use is present. Drug testing is used to monitor patients’ prescribed medications, as patients may under-report drug use to medical professionals, making some patients’ self-reports unreliable. Beechtree Diagnostics urine toxicology testing may be used to document abstinence for legal matters, disability determinations, custody disputes, or reinstatement in certain professions (e.g., lawyers, healthcare providers, professional athletes, airline pilots). Here are two points I like to share with you on how we stand out from the rest. Vacuum Tubes- Shipping urine in a cup result in spillage during the shipping process. We use vacuum tubes for urine as well as blood. Everything we supply you with has a port for the vacuum tube. This video is nice to show the importance of the vacuum tube https://lnkd.in/giSUyzk8 Subversion- We have patented process to catch Individuals trying to cheat a drug test. This is a multi-billion-dollar industry in the US. Approx 12% of samples we test are positive for one of the new ways to cheat a drug test. This video shows more information about subversion products. https://lnkd.in/gaKRMKki
Beechtree Diagnostics: "What makes us different"
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Weekly reads: MiMedX & Kimera Labs both get FDA warning letters, NYT deep dive on Bryan Johnson & the anti-aging movement, MUSE cell trial shows no benefit ...do the cells even exist? https://lnkd.in/guYXvVBw #stemcells #stemcell
Weekly reads: MiMedX & Kimera Labs FDA warnings, NYT on Bryan Johnson, MUSE cell trial - The Niche
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❗ EU Parliament emergency requests approved, with the vote on the amendment due Thursday 25th April 2024. ❗ Proposed amendments [from 24/01/24] includes: (1) MDR & IVDR: Measures to ensure market supply is uninterrupted as a result of the regulations and oversubscribed notified bodies. Manufacturers must issue notice to authorities signalling discontinuation or disruption of supply (addition of Article 10A). (2) Updated timelines (IVDR): - 31st December 2027 (Class D and IVDs under IVDD) - 31st December 2028 (Class C) - 31st December 2029 (Class B and A Sterile) (3) Quality Management Systems: - Mandatory and demonstrable implementation of QMS by the 26th May 2026 (4) Phased Approach for the Earlier Adoption of EUDAMED: - Mandatory use of several EUDAMED modules (including PMS) starts Q4 2025, followed by implementation of Clinical Investigations 2026 (Q3) through to full mandatory use by 2027 (Q4). Full commission proposal: https://lnkd.in/eGhCZqk5
#IVDR: EU Parliament emergency meeting today between 12:00-13:00 to discuss EU In Vitro Diagnostics Regulation transition timelines - including transitional impacts, new requirements and EUDAMED)
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Pretty large safety concerns IMO. Typically as you scale study design these safety concerns are amplified. ADC like Bispecifics are very powerful therapeutics and are uncontrollable. I’m always surprised at how many time’s scientists try the same thing expecting a different result. Any efficacy result is always suboptimal when it’s not safe.
Gilead, AstraZeneca/Daiichi Sankyo present mid-stage data on rival TROP2 antibody-drug conjugates
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Explore how our 3D spheroid cultures can revolutionize your anticancer drug screening. These complex models offer deeper insights into cellular interactions. Learn how we can support your research. https://ow.ly/Cq7T50Sq4AI #Drugdiscovery #spheroids #synergy #drugscreening
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The advent of the COVID-19 rapid antigen test launched at-home diagnostics to the forefront of conversation in the life sciences industry. Read about the top three issues developers of these tests should consider. https://lnkd.in/gfWVEY4K
Non-Lab Diagnostics: FDA Regulatory Considerations | MoFo Life Sciences
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Yes. You can discover your top drug candidate and fast-forward to IND. Whether you are pursuing a small molecule or biological therapeutic, our discovery solutions give you access to innovation, quick study starts, timely data delivery and scientific insights to progress from hit validation into IND/CTA and beyond. https://lnkd.in/eapJmPD8 #DrugDiscovery #DiscoveryToxicology #PKScreening #PharmacologyModels
Discovery
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