🔬💼Struggling to decide between RABS and Isolators for your aseptic manufacturing process? Look no further!🚀 ProSys Group presents our latest case study: RABS Vs Isolator - Choosing the Right Isolation Technology for You! Dive into the nuances of RABS and Isolators with our comprehensive study, tailored to help you make informed decisions aligned with your specific requirements💡 Here's a sneak peek at what our study reveals: - 🔹ProSys Group's integrated solutions streamline aseptic manufacturing reducing human intervention and enhancing product purity. 🔹Our expertise in designing, manufacturing, and validating Isolators and RABS systems ensures unparalleled performance and compliance. 🔹Discover how our solutions can transform your operations, optimising efficiency and elevating product quality simultaneously. Ready to make the right choice for your manufacturing process? Click the link to access the full case study: https://lnkd.in/eqZMMaXN Don't miss this opportunity to revolutionise your approach to aseptic manufacturing! 📞+353 21 4853900 🌐www.prosys.com 🗞 Check out ProSys Group newsfeed for all the latest and greatest in our industry >> https://bit.ly/41yTV1i << #ProSys #ProSysGroup #Aseptic #Sampling #Containment #AsepticManufacturing #Isolators #RABS #PharmaIndustry #PharmaceuticalIndustry #BiopharmaIndustry #BiopharmaceuticalIndustry #Innovation #CaseStudy
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Our comprehensive whitepaper demystifies the power of Single-Use efficiencies in room-to-room fluid transfer, optimizing productivity and cost-effectiveness. Explore how integrating disposable equipment accelerates operations while safeguarding controlled environments. Discover the impact of a sophisticated wall pass-through system, harnessing Single-Use components to mitigate contamination risks and streamline resource usage. DOWNLOAD our whitepaper and tap into the realm of efficient fluid transfer. https://hubs.ly/Q02cJYqj0 #asepticfluidtransfer #SingleUse #biopharma #pharma
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🧪🌡 Curious about the science behind keeping pharmaceuticals and research samples cold? Let's break it down! Lab refrigerators play a crucial role in preserving these valuable assets, and it all comes down to refrigerant flow through specific components. 🧊Here's a simple breakdown: It all starts with the flow of a special liquid called refrigerant. This process involves several key components: 𝟭. 𝗖𝗮𝗽𝗶𝗹𝗹𝗮𝗿𝘆 𝗧𝘂𝗯𝗲: The refrigerant enters through this narrow passage, lowering its pressure and temperature, thanks to friction, and decreasing its boiling point. 𝟮. 𝗘𝘃𝗮𝗽𝗼𝗿𝗮𝘁𝗼𝗿: Acting like a heat sponge, it absorbs heat and changes the refrigerant from liquid to gas. 𝟯. 𝗖𝗼𝗺𝗽𝗿𝗲𝘀𝘀𝗼𝗿: The gas is compressed, increasing pressure and temperature. 𝟰. 𝗖𝗼𝗻𝗱𝗲𝗻𝘀𝗲𝗿: Heat is released into the room, turning the gas back into a liquid for the cycle to start anew. In essence, your refrigerator cycles this special liquid, absorbing heat from inside and releasing it outside, ensuring pharmaceuticals and research samples are safe. Most lab refrigerators use a similar mechanism, known as "cold-wall" technology, with adaptations to meet performance requirements. Interesting to gain more insights into biopharmaceutical storage in pharmaceutical manufacturing? Join our upcoming webinar on November 8th, featuring industry experts: 🔹 Paul Sarrazin - Senior Consultant and Owner at P-care Solutions 🔹 Sylvain Riendeau - Vice President of Business Development Here's What You'll Gain: 🔸 Differentiate between traditional ULT and forced-air convection technology. 🔸 Integrate new advances in inventory and material-handling solutions into your workflow. 🔸 Leverage this new technology to protect sample integrity, improve yields, and conserve energy. Don't miss this opportunity to gain valuable insights into the future of cold storage in pharmaceutical manufacturing. 📈 Register now👉: https://rfr.bz/l6sq0tn 🌍 Proudly Sponsored by FARRAR™ - Powered by Trane Technologies FARRAR™ is dedicated to meeting the rapidly growing demand for low and ultra-low-temperature processes in the manufacturing, freezing, and storage of medicines, vaccines, and other life-science products. 🌐 #GMP #Pharma #Pharmaceutical #Pharmaceuticals #Quality #Pharmaceuticalmanufacturing #ColdStorage
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Choosing the correct excipient, lyoprotectant or cryoprotectant can be tricky when working with complex materials! Biopharma Group has over 30 years of experience when it comes to developing and optimising liquid and dried products. Some of the most common challenges that we see when it comes to choosing excipients include: ➡️ Compatibility with other ingredients ➡️ Biocompatibility and safety ➡️ Maintaining sample stability ➡️ Manufacturing and dose uniformity ➡️ Supply chain and availability of materials ➡️ Global regulatory requirements If you are experiencing any of these challenges then contact us today: https://bit.ly/3H9yivP #excipientselection #formulationdevelopment #freezedrying #optimisation #lyophilisation #liquid #compatibility #samplestability #BiopharmaGroup #CDMO
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Sr. Biosimilar Production Specialist at BGP | GMP | Six Sigma | Efficiently manufacturing bio-tech products.
Are you struggling to optimize your biosimilar production process? Understanding the nitty-gritty of biosimilar production isn't just about knowing how to use single-use technology. It takes an impressive grasp of quality standards, cost management, and leveraging data for error identification through Six Sigma principles. If your team lacks a deep understanding of these elements and the expertise to apply them effectively, it's time to revisit your strategies. Remember, inadequate grasp of these concepts can lead to a compromise in product quality and consequently, significant losses. Making sure you have the right blend of skills on your team can make all the difference in producing high quality biosimilars. Always strive for superior quality in biosimilar production—it's not just about the process, it's also about knowledge and application.
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Most pharmaceutical magnetically coupled mixers needs to secure that they rotate with a specific speed inside the tank, for this purpose most mixers have a speed sensor. The same mixers also needs to rotate in a specific direction, clockwise or counterclockwise to function properly. It is with this rotation direction the mixer is validated in the process. Most mixers today are operated with an AC induction motor, AC Induction motors easily change rotation direction during maintenance break or other stop or power breaks. If the batch is mixed with a mixer that rotates in the wrong direction the batch might need to be thrown away. Kest does not only offer a speed sensor, we offer a speed sensor system with logic incorporated, except from speed measuring, that system also secures that the mixer is rotating in the right direction. THIS IS PART OF OUR GREEN MIXING CONCEPT TO MINIMIZE WASTE! Stay tuned by following Kest on LinkedIn, click the link: https://lnkd.in/eKmXJYHm and click the “Follow” button. If you want to know more, visit http://www.kest.se #pharmaceuticalindustry #pharmaceuticalmanufacturing #pharmaindustry #pharma #biotech #biotechnologyindustry #biotechnology #biopharma #lifesciences
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🔍 The Importance of Filter Housing in Sterile Gas Filtration 🔍 In the world of sterile gas filtration, filter housings might appear simple, but their impact is profound. Quality, design, surface finish, and welding are paramount, yet the trust between manufacturer and client is equally vital. A meticulously crafted filter housing, designed with precision and tailored for specific operating conditions, ensures optimal long-term performance. This commitment to excellence significantly enhances user experience and reliability. At FSP Technologies, we take pride in manufacturing filter housings that meet the highest standards, because we understand the critical role they play in your operations. #SterileFiltration #QualityMatters #PrecisionEngineering #FSPTechnologies #Trust #ManufacturingExcellence #Pharmaceuticalindustry #injectables #Biopharmaceuticals #Filtrationindustry #beveragefiltration #API
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Traditionally, pharma producers relied on dry milling to produce API. However, as the potency of APIs increased, dry handling threw a curveball with significant challenges, leading to dust generation and product losses. On top of that, the tightening grip of safety regulations only exacerbated these issues. So, how can we improve API production? We had a great conversation with Werner Kanzinger, VP at IKA – Laboratory, Analytical and Process Technology, one of the first to use the wet milling method for API production. But what's the buzz about wet milling? It's all about controlling the growth of crystals during the crystallization step itself. 🙌 The result? Reduced dust, a hygiene facelift, meticulous particle size and distribution control, shorter production cycles, and enhanced cost efficiency. Curious to learn more? Dive into the full story at: https://lnkd.in/eUaRDpqj 🗓️🤝Don’t miss the chance to speak with the IKA team at CPHI on 24-26 October at stand 3T26, zone PMEC #cphi #cphi2023 #wetmilling #milling #apiproduction #api #activephrmaceuticalingredients #crystallization #particlesize #dispersing #pharma #pharmaindustry #pharmaceuticals
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🚏 NEW VIDEO 🎬 Associate Director for Single Use Technologies Ronan Healy walks us through a recent CPi Biotech advanced Single Use Bioprocess skid in our latest Video. ⬇ Check out this Single Pass Tangential Flow Filtration System (SPTFF), which we recently delivered to a US-based client. In Critical Bioprocessing applications, Single-pass TFF systems play a central role in improving manufacturing efficiency and productivity through the implementation of Single-Use Technology. Such Systems play a key part in the manufacture of lifesaving vaccines and critical therapeutics. With our SPTFF technology, our clients can achieve process intensification, volume reduction, and continuous manufacturing through the implementation of CPi Biotech Single-Pass Tangential Flow Filtration SYSTEMS. These systems can be deployed in many downstream unit operations, including clarification, chromatography, and final ultrafiltration steps. Significantly, CPi Biotech SPTFF systems save on valuable cleanroom production space by consuming a smaller footprint over traditional batch mode TFF systems. #bioprocessing #singleuse #modulardesign #videomarketing PSG, a Dover company Quattroflow, a PSG brand Watson-Marlow - UK-PendoTECH
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Crafted to meet the demanding needs of industries such as chemical, pharmaceutical, and food processing, our high vacuum systems stand as paragons of performance and versatility. Engineered to excel where conventional pumps falter, our systems ensure optimal vacuum capacity and gas handling, enhancing process efficiency across diverse applications. Whether it's evacuating air from sealed vessels or supporting sensitive research environments, our systems offer unmatched reliability and adaptability. With precise engineering and advanced technology, we provide tailored solutions to meet the unique requirements of each industry, ensuring seamless integration and operation. From maintaining sterile environments in pharmaceutical manufacturing to enhancing chemical processing efficiency, our high vacuum systems play a pivotal role in driving productivity and innovation. Trust in our expertise to elevate your operations to new heights of performance and reliability. #TMVT #WhatsYourTMVTFit #EngineeringExcellence"
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Product reveal 📣 We're excited to introduce our new bioreactor FERMI SKID BF50! A groundbreaking innovation for bacteriophage research & production developed by RENI in collaboration with JAFRAL Biosolutions – The leader in Bacteriophage research ! As antibiotics face declining efficacy, the need for specialized solutions is vital. We aim to support biopharmaceutical development in meeting evolving healthcare challenges, while also ensuring a sustainable production process. Key Features of FERMI SKID BF50: - Integrated Clean-in-Place (CIP) and Sterilize-in-Place (SIP) systems for optimal hygiene. - Automated purified water dosing and air brake valve for a streamlined process. - Bottom-mounted magnetic agitator for optimal mixing. - Fully GMP compliant software for regulatory compliance. - Clean room hygienic design. - New generation aseptic membrane valves for efficiency. - Clip-On temperature sensors for a hygienic process and validation. - Shorter CIP cycle time, minimizing downtime and maintenance hassles. - Efficient and safe. Choose RENI as your reliable partner in Engineering the Future of Bio-Processes. #FERMISKIDBF50 #Biopharmaceuticals #Innovation #BacteriophageProduction #EngineeringTheFuture #BioProcesses #JAFRAL #RENIEngineering #Bioreactor #Fermenter #processengineering #system #laboratory #future
RENI FERMI-SKID BF50 Bioreactor
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