JRF Global’s Post

Revolutionise Your Drug Testing Today! Say goodbye to multiple tests! Our Drugs of Abuse Hair Array on the Evidence Investigator lets you detect 10 drugs & metabolites from just one hair sample! 💇♀️ ⚡ Key Features: ✔️ One hair sample, multiple drugs tested! ✔️ Detect and analyse patterns of illicit drug use ✔️ Run multiple samples at once for ultimate efficiency Don’t settle for less—get faster, more accurate results with the latest drug testing technology! To find out more, visit our website or email us 👇 ✉️ info@randoxtoxicology.com 🌐 https://lnkd.in/dbwY5Mn7 #toxicologytesting #drugtesting #DrugsOfAbuse #forensictesting #forensictoxicology #hairtesting

In the fast-paced world of pharmaceutical and biotech industries, stability is key. One challenge many companies face is training in-house toxicologists, only to lose them to another opportunity. This turnover can disrupt productivity, increase costs, and create knowledge gaps in your team. With OEL Fastrac+, you can gain consistent and reliable access to all your OEL/ADE values without the uncertainty of turnover. Our service delivers expert toxicological support without the need for extensive in-house training. You’ll have peace of mind knowing that your compliance needs are always met by a trusted team of toxicologists. ✅ Save time ✅ Optimize spending ✅ Maintain process stability Reach out to Joanne Low or Peter Burke to learn more about how OEL Fastrac+ can help streamline your operations and eliminate toxicological guesswork. #Toxicology #Pharma #pharmaceuticalmanufacturing #Compliance #WorkplaceSafety

Register for our next webinar in our Comprehensive Answers webinar series, which will feature Faye Caldwell presenting on "The Use of Oral Fluid Drug Testing in DOT Regulated Workplaces." The webinar will be on October 15, 2024 at 11:30 AM CST - definitely worth checking out! #toxicology #oralfluiddrugtesting #freewebinar #abbottproud

In 2023, the U.S. Department of Transportation (DOT) published the final rule amending the DOT's regulated industry drug testing program to include oral fluid testing. During the next webinar in the series, Faye Caldwell will provide a detailed overview of the new rules. During the presentation, Faye will not only highlight the practicalities and timing of oral fluid, but also other important changes with a focus on what employers and service agents can do to prepare for these changes. Register below to the webinar 👇 #toxicology #freeeducation #abbottproud #oralfluidtesting

This one will be awesome. It’s the #1 topic I hear about in #transportation. If your business has any DOT regulated employees, you will not want to miss this webinar next week on the use of #oralfluid #drugtesting. #abbottproud

🚨 Nearly 90% of clinical trials fail! 🚨 The 2nd biggest reason (after efficacy), impacting approx. 30% of trials, is toxicity. ⚠️ When side effects are too severe, even promising drugs can’t move forward. Reasons include: 🔍 Early pre-clinical studies often miss side effects that appear in human trials. 🔍 Toxicities can emerge when tested in large and diverse populations. 🔍 Aggressively pushing doses without fully understanding limits leads to toxicity risks. #ClinicalTrials #DrugDevelopment #Biotech #Toxicity #Pharma #ClinicalResearch #SafetyProfiles

As a foundational part of IND-enabling studies, acute toxicity testing provides vital safety insights on drug candidates. From identifying optimal dosing, and characterizing exposure-response relationships to setting safety limits and spotting potential adverse effects, these studies help define safe dose ranges for initial human trials. They’re crucial in mitigating early risks, ensuring a smooth transition from preclinical research to clinical trials. With over 40 years of experience, JRF Global is a trusted preclinical CRO with a strong legacy in IND-enabling studies. If your program requires support with IND-enabling studies, let’s connect—our team is ready to assist you at every step. #INDEnabling #PreclinicalResearch #CRO #DrugDevelopment #AcuteToxicity #JRFGlobal #toxicity #efficacy #safety #drug #regulatorysubmission #preIND

The regulatory landscape for e-liquid products in the United States has become increasingly stringent. Recent reviews by the U.S. Food and Drug Administration's (FDA) Centre for Tobacco Products highlight the necessity for manufacturers and distributors to comply with the Federal Food, Drug, and Cosmetic Act (FD&C Act). To know more details regarding the Navigating FDA regulations for E-Liquid Products, please click the below link and follow Maven Scientific Laboratories Pvt Ltd for more interesting updates. https://lnkd.in/gJ6A2hJu #FDA #ELiquid #Vaping #TobaccoRegulations #Compliance #RiskManagement #Toxicology #PublicHealth #MavenScientific #RegulatoryAffairs #EliquidManufacturers #HealthSafety

🪴As cannabis use becomes more prevalent and legal restrictions ease, the need for reliable cannabis intoxication testing is more critical than ever. While various biological matrices—such as urine, blood, sweat, hair, and oral fluid—can identify prior use, they each have limitations in assessing current impairment, a crucial factor in many jurisdictions.  💨 Exhaled breath has emerged as a promising matrix for detecting recent use. However, challenges remain, including uncertainty around breath levels that indicate impairment and the technical hurdles of rapid, on-site analysis. The short intoxication window of cannabis compared to its presence in the body further complicates effective screening. 📖 https://lnkd.in/dXdjh62D This review sheds light on the current landscape of cannabis intoxication testing, highlighting both the challenges of existing forensic techniques and the growing interest in breath analysis from researchers and commercial entities alike. As we navigate this evolving field, robust solutions for rapid toxicological screening are essential for public safety. 💡In the meantime, while research and science search for the best suiting methodology, please be aware that cannabis use and driving or operating heavy machinery might be dangerous, does is to be completely avoided. #CannabisResearch #PublicSafety #ForensicScience #Toxicology #Health #SafeLevels #CannabisCommunity #CannabisIndustry #CannabisEducation

Brace yourselves! The FDA recently dropped a bombshell on the medtech industry. Fraudulent testing data is putting patient safety at risk, and it's our job to sniff out the bad apples. The FDA's inspected non-clinical GLP lab database is a great resource for vetting third-party labs. (Link in comments) But I want to hear from you: What other tools or strategies do you use to ensure data integrity? Drop your tips below, and let's keep this industry clean! Spread the word by sharing this post - more eyes on this issue means better solutions. Let's rally together and demand transparency! #PatientSafety #MedTech #MedicalDevices #DataIntegrity #FDACompliance #QualityAssurance #ThirdPartyTesting #GLP #Transparency #MedTechCommunity #Biocompatibility #Toxicology #NonClinicalTeating #CRO #QualityEngineering #DeviceSafety #SocietyOfToxicology