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Dive into insightful research comparing manual cleaning to chlorine dioxide gas decontamination in the International Society for Pharmaceutical Engineering Journal. Explore findings from the Bausch+Lomb Vision Care facility in Greenville, SC, revealing the unparalleled coverage and effectiveness of chlorine dioxide gas. Plus, gain valuable insights into equipment, process, and cost comparisons. Spoiler alert: the results are impressive! Download the full article below. https://ow.ly/oWy450Rm4U0 #Decontamination #ChlorineDioxideGas #BiomedicalResearch #VivariumManagement

#Guide: How to problem solve for complicated #polymer and rubber container closure systems and deliver Extractables & Leachables study success. Get your insights: https://lnkd.in/eQrPM5bv #pharmaceutical #PharmaceuticalIndustry #ExtractablesLeachables #WhitePaper

Apex® Biological Indicator (BI) products are designed specifically to meet the unique needs of the pharmaceutical, food, and medical device industries utilizing vaporized hydrogen peroxide (VH2O2) decontamination. The Apex® product line offers: The most resistant strain to VH202 process to assure the manufacturing area is decontaminated Greatly reduced false positives because products match the decontamination process A highly flexible portfolio of BI’s to match the resistance of process parameters Whether it be stainless steel discs/ribbons or a spore suspension, Apex® BI products offer the ideal solution to monitoring hydrogen peroxide decontamination, utilizing vaporized hydrogen peroxide (VH202) decontamination. Mesa Laboratories, Inc., Pharmaceutical Online #vaporhydrogenperoxide #sterilization #pharma #decontamination #pharma #qualityassurance Dan Johnson, Crystal Sgrignoli Hostler, Megan Wood

In this new Pharmaceutical Online article, Yadnyesh Patel continues his article series on #sterilityassurance by discussing nine key contributing factors for maintaining sterility assurance, such as decontamination, facilities, materials, and personnel. https://lnkd.in/ewdAHWYq #pharma #biotech #drugmanufacturing

Introduction on E&L for the pharmaceutical sector > Extractables: Compounds extracted or forced out of container closure system materials and components under fairly aggressive experimental conditions. --> Scope of extractables screening → assess what MIGHT migrate >Leachables: Chemical entities, organic or inorganic, that leach into the drug product under normal conditions. Patients can be exposed to leachables during normal use of a drug product, therefore leachables are of potential safety concern. They are are typically a subset of extractables or are derived from extractables.   -->Scope of leachable screening → assess what DOES migrate For more information see our brochure and contact our team of experts https://lnkd.in/dpAMKUT4 #neotron #packaging #pharma #extractable #leachable

Impurities & Crystallization in Pharmaceutical & Chemical Compounds A new 1:1 co-crystal of salicylamide and salicylic acid, referred to as Co-Crystal Form II, was discovered. This form is thermodynamically more stable than the previously known Co-Crystal Form I at higher temperatures. The findings highlight how the presence of a second component (such as impurities) can significantly alter the thermodynamic stabilities of polymorphs, potentially leading to the appearance or disappearance of certain polymorphic forms. This has important implications for polymorph screening and the development of pharmaceutical processes. Link to the article for more information: https://lnkd.in/gEzCNYty #PharmaceuticalResearch #Crystallography #Polymorphs #DrugDevelopment #Crystallization #ResearchInnovation

𝗧𝗵𝗲 𝗣𝗼𝘁𝗲𝗻𝘁𝗶𝗮𝗹 𝗳𝗼𝗿 𝗮 𝗕𝗮𝗻 𝗼𝗻 𝗧𝗶𝗢𝟮 (𝗘𝟭𝟳𝟭) 𝘂𝘀𝗲 𝗶𝗻 𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗲𝘂𝘁𝗶𝗰𝗮𝗹𝘀 - See the latest Technical Newsletter by Fuji Chemical Industries Co., Ltd. Fuji Chemical Industries USA, Inc and read the article ➡️https://lnkd.in/ehMaiXQU #pharmaceutical #excipients #tio2

Filtration processes in Biosiimilars: Cross-flow filtration is a widely used technique in the pharmaceutical industry for separating, purifying, and concentrating substances in liquids. It involves passing a liquid mixture through a specialized filter with a tangential flow. As the liquid flows across the filter surface, the smaller molecules pass through the membrane while larger molecules, particles, or contaminants are retained. This process helps in purifying and concentrating pharmaceutical products, separating biomolecules, removing impurities, and ensuring product quality in various stages of drug development and manufacturing. #biosimilars #manufacturinginnovation #newideas #innovation #mediaproduction #filtration

How do pharmaceutical businesses ensure that they recover maximum amounts of active compounds during the manufacturing processes - while keeping the quality of product consistently good, and cost-economics positive? Learn in this case study where we uncover - - Challenges faced by pharma businesses while recovering active compounds from wastewater steams? - How is the quality of the compound kept consistent and good? - How Permionics designed and delivered a customized solution to address these challenges - Details of technologies implemented, processes followed, and results Download Case Study: https://lnkd.in/dzk73Wtq

The PH2-750 is the perfect solution for pharmaceutical companies looking for a machine with a medium-to-high production capacity and flexibility in terms of production. Key features for pharmaceutical applications: 🔵 Aseptic or Ultra-Clean blowing system made of stainless steel/ptfe pipes. 🔵 Fan filter unit: an essential system to guarantee clean air and contamination control. 🔵 Extraction Unity: extracts the dust generated during the production cycle. 🔵 Large use of inox components. Would you like to know more technical features about the PH2-750? Download the datasheet: https://lnkd.in/d6yZ6j2g #pharma #pharmaceutical #manufacturing #efficiency #blowmolding #aseptic