Qualio’s Post

Are you Ready for the future of validation? The Res_Q platform is the world's leading-edge life sciences validation platform. Intelligent, scalable, and built for the future, Res_Q accelerates validation and helps your organization manage the risk - and complexity - that comes with larger and larger tech stacks. Book a demo today! https://lnkd.in/g77787vm #computersystemvalidation #computersystemassurance #lifesciencescompliance #lifesciences #biotechnology #gxp

The biopharma industry is shifting away from traditional batch manufacturing to continuous alternatives. This continuous approach enhances manufacturing methods by reducing waste, minimising labour needs and lowering risk. As part of this continuous process, leveraging process analytic technologies (PAT) provides real-time analysis to ensure a product meets the critical quality attributes (CQA) and is safe for patients in accelerated time frames. To learn more about how PAT is elevating continuous RNA manufacturing, explore the recent article by ReciBioPharm’s Head of Process Analytics and Data Science Edita B. Click here: https://lnkd.in/ddD8FDuJ #continuousmanufacturing #processanalytictechnologies #quality

Excited to share a case study where our team delivered comprehensive inspection readiness and remediation support for a CMO facing significant challenges in quality production and batch release delays. Our experts conducted a thorough gap assessment, reduced backlog deviations, and implemented a robust investigation system, enhancing their QMS and significantly reducing batch release timelines from 300 days to just 30. 🏆 ________________ Check out the slides below to see how we made it happen! #iPharmGxP #biotech #casestudy

Thank you to those who attended today's Bioprocess Online's Live Event, "Single-Use Technologies for Bioprocessing: An Essential Update". Major thanks to Mark Petrich and Paul Priebe for being our industry experts! If you did not have a chance to hop on and listen, you can catch the on-demand recording here: 👂 https://lnkd.in/gtwECgkp If you were left hanging and wanted to ask the experts more questions, please leave your question below. ⬇ #singleuse #supplychainsecurity #regulatory

Industrial biotechs use Scispot to streamline everything from strain optimization to batch tracking and regulatory compliance—all in one platform. 👨🔬 Scispot’s automated workflows catch bottlenecks early, track data across each production stage, and ensure full traceability for audits. With all processes connected, industrial biotech teams can scale faster and focus on advancing their research and production goals. Read through our carousel to see why Scispot is the ideal choice for industrial biotech labs ready to streamline, scale, and succeed. 👉 Book a demo today: https://lnkd.in/g6tvXT9Q

CTOs, let's shatter some common bioprocessing myths! Myth 1: Process Variability is Inevitable – No more! It's manageable with the right strategies. Myth 2: Process Control is Just for Compliance – Wrong! It's your key to consistent product quality. Myth 3: Regulatory Compliance is a Necessary Evil – It's your roadmap to success, embrace it. Break free from these myths, CTOs! Your bioprocessing journey deserves a clean slate. #cellculture #processdevelopment #bioprocessing #celltherapymanufacturing #cellandgenetherapy #leadbiotech

Dive into the era of battery-powered data loggers with our latest Blog Post, "Kaye's Time Warp: Battery-Powered Data Loggers." In the early 2000s, Kaye advanced to integrate wireless, power-efficient data loggers, marking a pivotal moment in thermal process validation. Discover how we overcame challenges related to accuracy, reliability, seamless data collection, and how we adapted to emerging regulations. This blog will take you on a journey through the evolution of our innovative tech solutions, ultimately leading to our robust Kaye ValProbe RT system. Don't miss the opportunity to learn more about our continuous commitment to innovation, customer's need focus, and vision for the future. Take a leap back in time with us and see how far we've come! Dive in here: https://lnkd.in/eJzaDZ4T   #Kaye #DataLoggers #WirelessTech #PharmaceuticalInnovation #ContinuousMonitoring #ThermalValidation #GxP #KayeValProbeRT #Pharma #Biotech #Pharmaceuticalindustry #Biotechnology

Clinical phase technology transfer While most discussions are around the transfer to commercial scale manufacturing, it should be remembered that process and assay information (tech) transfer also occurs at all points through a products life cycle from development to production end of life, including through the clinical trial phases. My latest memo looks at the technology transfer at the clinical trial stages. https://lnkd.in/gBFn72pu

Are you a Life Sciences company ready to transform your GxP validation and compliance using leading-edge technology with AI-supported toolsets? If so, it's time to demo Res_Q: the premier Life Sciences validation solution that automates, unifies, and accelerates all of your validation processes. Book a demo today to see how Res_Q can add value, improve efficiency, and ensure complete audit-readiness around the clock. https://lnkd.in/g77787vm #biotechnology #lifesciences #computersystemvalidation

Speed is a necessity. How are Resilience teams developing platforms to accelerate vector development & manufacturing? Learn from Xiaotong Fu, our Head of Downstream Process Development and Pilot Operations, as he shares how his team leverages modular platforms and collaborations with our GMP Manufacturing team to ensure Resilience can deliver a GMP batch of viral vector in 12 months or less. Watch the full interview on our blog: https://hubs.ly/Q02DCgGl0