RIBOSOME RESEARCH CENTRE PVT. LTD.’s Post

"Wishing you a New Year filled with joy, laughter, and countless moments of happiness! May each day be a new opportunity for growth, success, and love. Here's to new beginnings and endless possibilities in the coming year. Let's embrace the challenges, celebrate the victories, and make every moment count. Happy New Year to you and yours! 🎉✨" #NewYear #FreshStart #2024Goals #NewYear #newyears # #newyearsresolution #rrc #preclinical #nonclinical #pharmaceutical #analyticalchemistry #chemistry #toxicology #invivo #invitro #glp #pharmacology #medicaldevice #agrochemical #pesticide #microbiology website link : https://lnkd.in/duuPi7rA

🚀 Our Toxicological Risk Assessment Centre of Excellence (TRACE) offers top-tier support in product safety and occupational toxicology for pharmaceutical, biotech, and medical device companies globally. We excel in qualitative and quantitative health assessments, crucial for product development, manufacturing, and post-marketing. Navigating ICH, FDA, EMA, and WHO regulations is our specialty, ensuring safe levels for contaminants and impurities. From Health-Based Exposure Limits (HBELs), including Occupational Exposure Limits (OELs), to Nitrosamine Assessments, our board-certified toxicologists ensure that all assessments are scientifically justified and compliant with regulations. To learn more email us at trace@intertek.com or visit: https://lnkd.in/esyedYMD #Toxicology #ProductSafety #OccupationalToxicology #Pharmaceuticals #Biotechnology #MedicalDevices #RegulatoryCompliance #IntertekAssuris #RiskAssessment #PDE #OEL #OEB #HBEL #ICHM7 #Impurities #Leachables #Extractables #Nitrosamines

Industry experts from Smithers and bibra toxicology advice & consulting are presenting on medical devices and medicinal products on Thursday 27 June - have you registered yet? This webinar will cover the origins of E&L, terminology, regulatory frameworks including ISO 10993-18, USP and other guidance, toxicological risk assessment, chemical characterization best practices, experimental techniques, and more. Gain valuable insights into interpreting toxicological risk assessments, understanding thresholds, and optimizing study design for extractables and leachables analysis. More information: https://lnkd.in/eKQuuBEN Book your ticket: https://lnkd.in/eM-FuxYv Smithers - Market Intelligence Services #eandl #meddevices #biopharma #pharmaceuticalindustry #respiratorydevices #event #respiratory #pharmaceutical #pharmadevices #designofexperiment #medical #team #projectmanagement #doe #medicaldevices #fda #usp #pharmaceuticals #prefilledsyringes #combinationdevices #syringes #testing #syringe #technology #medicaldevice #transport #elastomericclosures

"May the divine presence of Ramlala Murti Pran Pratishtha fill your hearts with joy, peace, and eternal blessings on this auspicious occasion, courtesy of RRC." #RamlalaPranPratishtha #DivineRamlala #RamlalaBlessings #SpiritualMileston #DivinePresence #RRCWishes #RamlalaMurtiCelebration #preclinical #nonclinical #pharmaceutical #analyticalchemistry #chemistry #toxicology #invivo #invitro #glp #pharmacology #medicaldevice #agrochemical #pesticide #microbiology website link : https://lnkd.in/duuPi7rA

💥 The FDA recently released draft guidance on the purpose and content of Use-Related Risk Analyses (#URRA) for drugs, biological products, and combination products. 📑 This guidance assists in determining human factors data needs during product development and supports marketing applications. Let’s check the key points of URRA development: ▶ Identifying User Tasks: Determine all tasks that users will need to perform. ▶ Identifying Potential Use Errors: Analyze potential errors that could occur during these tasks. ▶ Evaluating Potential Harms: Assess the potential harm resulting from use errors. ▶ Categorizing Tasks: Differentiate between critical and non-critical tasks. ▶ Risk Controls and Evaluation Methods: Develop strategies to control risks and methods to evaluate their effectiveness. Comments on the draft guidance are possible until 09.09.2024! Follow us for regulatory updates and scientific insights! 💻www.toxhub-consulting.com 📩 info@toxhub-consulting.com #ToxHub #Consultancy #Pharmaceutical #Drugs #Toxicology

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https://lnkd.in/gbkjiSaq Article Title: Glass Delamination in sterile formulations and Drug Recalls: A Review Author(s): Kabirdas B Ghorpade* and Sharda M Shinde Journal: International Journal of Pharmaceutical Sciences and Developmental Research Journal ISSN: 2640-7760 Abstract: Injectable formulations are constantly facing continuing challenges of glass compatibility. To assure glass compatibility of the injectable formulation in the area of current interest. Most of the common and serious challenges of glass compatibility are glass delamination. Glass delamination is basically the degradation of the glass and formation of the flakes as a result of the incompatibility with the product stored. The other factors which contribute to glass delamination are the Type of glass container used, Storage condition, and Pharmaceutical Processings like terminal sterilization. Glass delamination should be taken very seriously as it is when present in the formulations it is directly related to the health of the patient. This review describes the Factors responsible for the glass delamination and its effect on patient health and the quality control analysis techniques of the same. #Glassdelamination #Terminalsterilization #Hydrolyticresistance #SEM #TEM #Drugrecalls #MedicinalChemistry #DrugDevelopment #Pharmacokinetics #Pharmacodynamics #Pharmacogenomics #Toxicology #Pharmaceutics #Biopharmaceutics #Pharmacognosy #PharmaceuticalChemistry #PharmacyPractice #CommunityPharmacy #HospitalPharmacy #IndustrialPharmacy #RegulatoryAffairs #DrugFormulation#DrugDelivery #PharmacyManagement #PharmaceuticalTechnology #PharmacyEducation #ClinicalTrials

Join us for an insightful webinar covering the origins of E&L, regulatory frameworks like ISO 10993-18, USP guidance, toxicological risk assessment, and chemical characterization best practices. Gain valuable insights into interpreting risk assessments, understanding thresholds, and optimizing study design for extractables and leachables analysis. Register here: https://lnkd.in/enCpGt3h Smithers - Medical Device Testing

Do you know - EviaSearch, www.eviasearch.com gives you INSTANT results with the LIST of 'Right-Fit' Service Providers? Yes, this is true, in just 3 clicks in less than a minute, you can get the LIST of 'Right-Fit' Service providers - specific to your Query. No Pop-ups, No -clutter, No unwanted listing, ONLY specific results. Experience the Difference, use EviaSearch!! If you need any assistance, please write to us at charmi@evisearch.com #pharma #pharmaceuticalindustry #pharmaceuticalmanufacturing #cros #eviasearch #contractmanufacturing #thirdpartymanufacturing, #clinicalresearch #clinicaltrials #toxicology #laboratory #bioavailability #serviceindustry #searchengine #consultingservices #consulting #consultants

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