Christina Pecoraro

With the #FDA and #EPA pushing for a change, the medical device industry is exploring alternative #sterilization technologies to EtO. Explore five of these promising alternatives that could revolutionize sterilization practices while ensuring safety and compliance: https://bit.ly/3DvN8ep

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Is the blue dye test the best option for blister pack leak testing? Learn about its limitations and why other methods may be more effective! #BlisterPackTesting #LeakDetection #BlueDyeTest https://lnkd.in/gnXej4aX

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The CELERITY™ HP Chemical Indicator Challenge Pack provides a consistent, thorough method of confirming sterilant penetration in conformance with ISO 22441. Validated for use in all V-PRO™ Low Temperature Sterilization Systems. Learn More Here: https://bit.ly/3LmypGg

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Biological Sterilization Indicating Equipment Market 2024-2032: Global Research Report. Request for Sample Copy: https://lnkd.in/dpwJuf5W The Biological Sterilization Indicating Equipment Market is set to experience significant growth, fueled by advancements in sterilization validation technologies and stringent healthcare regulations. This market was valued at approximately USD 4.5 billion in 2023 and is projected to reach USD 7.8 billion by 2032, growing at a robust CAGR of 6.5% during the forecast period. Biological indicators are crucial in ensuring the efficacy of sterilization processes, particularly in critical sectors such as healthcare, pharmaceuticals, and food safety, providing unmatched reliability in infection control. Our latest report delves into both quantitative and qualitative insights into this market, covering key manufacturers, regional analyses, product types, and applications. It also profiles leading companies, highlighting product offerings and market shares, helping stakeholders make informed decisions in this growing sector. Examination of manufacturing trends and innovations in sterilization validation systems. Regional market dynamics, with detailed segmentation by North America, Europe, Asia-Pacific, South America, and the Middle East & Africa. Application-specific growth trends, particularly in pharmaceutical sterilization and medical device disinfection. Segment-wise growth forecasts and consumption value trends are presented for 2024-2032, enabling businesses to identify and target lucrative market niches for expansion. For more details, request a sample copy of the report. To Know Global Scope and Demand of Biological Sterilization Indicating Equipment. Request for Sample Copy: https://lnkd.in/dpwJuf5W By Type: Biological indicators, self-contained indicators, spore-based indicators. By Applications: Healthcare facilities, pharmaceutical manufacturing, food and beverage sterilization. By Regions: North America, Europe, Asia-Pacific, South America, Middle East & Africa. By Key Players: 3M, Cantel Medical, Mesa Laboratories, Inc. STERIS, Sartorius, Getinge, Cardinal Health, Terragene, MATACHANA, Tuttnauer, Belimed, Andersen Sterilizers, Advanced Sterilization Products, Sterigenics, Crosstex International, Propper Manufacturing Company, Inc., Noxilizer, Inc., Johnson & Johnson, Biotest AG, VWR, part of Avantor, Metrex, Medical Innovations, Steritec, Olympus Corporation, Stericycle. #biologicalsterilization #infectioncontrol #healthcareinnovation #sterilizationequipment #medicaldevices #pharmaceuticalindustry #biologicalindicators #sterilizationvalidation #healthcaretrends #pharmaquality #foodsafety #cagr2024 #medicaltechnology #emergingmarkets #innovationinhealthcare #globalmarket2024 #healthcaregrowth #sterilizationsolutions #biologicalsafety #marketreport

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Are you attending RAPS Convergence 2024? Visit Element Materials Technology booth 642 and just ask for Kim Lipman to see how the RegNav tool identifies product-level requirements for medical devices faster than ever before! #RAPS2024 https://ow.ly/ejIY50TljA1 #RegulatoryCommunity #RAPSConference #Regulations #Compliance #HealthcareRegulation #MedicalDevices #RegulatoryAffairs #RegulatoryCompliance #ElementMaterialsTechnology #ElementRegNav #RegNav

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🚨 Last Chance to Register! 🚨 Our webinar, "Lab Automation Made SIMPLE: Understanding Automated Sample Aliquoting," is happening on Sept 5th. Don’t miss out on learning how the Scinomix AQ system can transform your lab. 🔗 Register Now: https://hubs.ly/Q02M3Pfk0 #LabAutomation #Scinomix #Webinar #Aliquoting

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As regulatory pressures and environmental concerns grow, the medical device and pharmaceutical industries are evolving sterilization methods. While ethylene oxide (EO) has been a staple for decades, the future calls for safer, more sustainable alternatives. In our recent article with Healthcare Packaging we explore: ✅ New techniques like beta irradiation, vaporized hydrogen peroxide (VHP), and x-ray technologies. ✅ EO’s environmental impact and stricter compliance demands. ✅ Strategies for manufacturers to ensure patient safety and product quality. Read more about how companies are leading this transformation. https://lnkd.in/eMJCPJex #Sterilization #MedTech #Sustainability #AscentialTechnologies

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As regulatory pressures and environmental concerns grow, the medical device and pharmaceutical industries are evolving sterilization methods. While ethylene oxide (EO) has been a staple for decades, the future calls for safer, more sustainable alternatives. In our recent article with Healthcare Packaging we explore: ✅ New techniques like beta irradiation, vaporized hydrogen peroxide (VHP), and x-ray technologies. ✅ EO’s environmental impact and stricter compliance demands. ✅ Strategies for manufacturers to ensure patient safety and product quality. Read more about how companies are leading this transformation. https://lnkd.in/eMJCPJex #Sterilization #MedTech #Sustainability #AscentialTechnologies

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Struggling with chemical inventory management and regulatory reporting? Learn how to streamline your processes and enhance fire safety https://bit.ly/3Q4JxdC #laboperations #labsafety #EHS #labcompliance

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As PFAS regulations tighten, the medical device industry faces new challenges and opportunities. Discover how these changes are reshaping the landscape and how to adapt in the latest Inside Battelle blog from our expert Shalene Thomas: https://okt.to/BoEzwZ #emergingregulations #pfaslifecycle #pfasalternatives #pathtoPFASfree

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Reevaluate Your Blister Pack Leak Testing: Uncover the Limitations of the Blue Dye Test! Discover why this traditional method might fall short and explore more advanced techniques for ensuring product integrity. #BlisterPackTesting #LeakDetection #BlueDyeTest https://lnkd.in/g3ke9kjC

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Reevaluate Your Blister Pack Leak Testing: Uncover the Limitations of the Blue Dye Test! Discover why this traditional method might fall short and explore more advanced techniques for ensuring product integrity. #BlisterPackTesting #LeakDetection #BlueDyeTest https://lnkd.in/g3ke9kjC

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Did you know the FDA now classifies Vaporized Hydrogen Peroxide (VHP) as an Established Category A method of sterilization for medical devices? Join us for a complimentary webinar to learn the latest VHP sterilization regulations and explore key characteristics, applications and validation requirements. Register here - https://lnkd.in/eCw9ZEjp #VHP #Sterilization #RegulatoryCompliance #STERISWebinar

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A Closer Look at ISO 13485 for Medical Device Manufacturing. Sacramento Manufacturers! If you happen to be (or contemplating being) a medical device manufacturer, take five minutes and read the story below from our partners CMTC. For medical device and equipment manufacturers, ISO 13485 does more than just specify important items for your QMS — it’s an easy way to signal to your customers that you’re willing to go above and beyond their basic expectations to ensure that you are producing high-quality, quality-conforming products. It also shows your partners and suppliers that you’re committed to monitoring and taking action to drive improvements through your supply chain. #madeinCA #cmtc #cmta #svma #gobiz #medicaldevicemanufacturing #advancedmanufacturing #manufacturing #careertraining #communitycollege #California #education #skillsdevelopment #workforcedevelopment #jobtraining #careerchange #cteeducation #manufacturingexcellence #manufacturingtraining #manufacturingcareers #ISO13485

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There are many factors to consider when choosing a material for your medical device. It must be sterile, among other requirements. Learn how to select a material that complies with healthcare regulations in this article from PlasticsToday: https://ow.ly/HayZ50Tpp33. #MedicalDevice #Healthcare #Silicone #Rubber

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Establish a detailed directory of laboratory equipment for the entire organization with related documents and records, authorized users, and maintenance/calibration history. Learn more at https://bit.ly/3WuKuj6 #laboperations #labsafety #EHS #labcompliance

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While the recent FDA Final Rule related to In Vitro Diagnostics and Laboratory Developed Tests has sparked concerns around enforcement risk, cost, and compliance burden for manufacturers, in our latest whitepaper we also highlight the hidden market access opportunities for IVD developers that are quick to adapt. Our experts Nayan Ghosh & Emma Feinerman draw parallels to a similar guidance around in vitro companion diagnostics released a decade prior, when companies like Foundation Medicine & QIAGEN saw favorable, product-specific coverage determinations by proactively pursuing FDA premarket review ahead of their LDT competitors. Request a full copy here: https://lnkd.in/eptbRN73

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