Rentschler Biopharma’s Post

Discover precise screening. Infinity Vibro Sifter CGMP uses the Gyro principle for dust-free screening in various sectors. Engineered for efficiency and ease, it offers smooth operation and easy maintenance. Contact us: +91 91463 30555 #InfinityMachines #engineeringexcellence #pharmaceuticalmachinery #industrystandards #precisionengineering #qualityproducts #productivityboost #manufacturing #innovations #pharmaautomation #smoothoperation #industrialinnovation #processoptimization

Looking for a robust CHO cell line platform with companion media and feeds? Look no further than CHOZN-UCOE combined platform to.. 1. Accelerate your cell line development by increased efficiency of isolating high producing clones. 2. Increase cell line development success with hard-to produce molecules. 3. Achieve high and stable titers to expedite your cGMP manufacturing with fewer resources. This brochure illustrates usage of UCOE platform in combination with CHOZN GS-/- cell line and benefits of usage.

Need optimally designed, cGMP grade synthetic controls to ensure the dependability and accuracy of your molecular tests? Our OEM service has custom manufacturing capabilities to accommodate different sequence, concentration, filling, and labeling needs. Learn more: https://bit.ly/4aJG50M #molecularcontrols #moleculardiagnostics #diagnostics #controls #infectiousdisease #moleculartest

Single System; multiple applications: virus inactivation, virus filtration, depth filtartion, NFF !! Customisable, as per need of regulatory compliance !! #regulatorycompliance, #21CFR, #GMP, #automation !!

mAbs scale-up from research to full-scale manufacturing Scaling up from research-grade raw materials to full cGMP quality should be seamless, not siloed. That means planning well in advance is critical. At Avantor, we understand the complexities, as well as the quality and regulatory requirements, you need to succeed and are here for support. No more sleepless nights worrying about delays; reach out to learn more about our proactive approach to quality as you scale. Learn more.. https://lnkd.in/gCGdHBVi

🕵️ Curious to discover how to unlock the potential of vaccine manufacturing? Watch this on-demand webinar unveiling how to address scale-up challenges through technological innovation for cost-effective vaccine development 💉 What will you learn? ▪️ How scalable-by-design fixed-bed technology overcomes limitations of traditional methods for rapid process transfer. ▪️ A CDMO technology transfer, optimized and scaled up in under 8 months. ▪️ Making cGMP vaccine manufacturing accessible globally, reducing costs, and boosting production capacity for decentralized manufacturing. Watch the webinar now 👉 https://lnkd.in/ePA_xujm

🧑🔬Ensuring the CDMO you Choose is RIGHT for you 🔬Quality is paramount in pharmaceutical development, impacting not just regulatory compliance but also cost, time, and patient safety. Check out Onyx Scientific in the link below to find out why we're right for you! 1) Evaluating a CDMO's quality involves examining their processes, organizational commitment, and adaptability. Effective processes ensure product quality, safety, and compliance while supporting proactive quality management. a CDMO should prioritize efficiency through well-designed processes and a trained workforce, utilizing an electronic quality monitoring system (EQMS) for transparency and cost-effectiveness. 2) A strong organizational commitment to quality fosters a culture where excellence is prioritized across all levels, with Quality Assurance (QA) acting as a mentor rather than a police force. This culture ensures that every team member is responsible for maintaining quality, supported by leadership's dedication to high standards. 3) Proactively managing quality issues and continuously improving processes are crucial for a CDMO. A CDMO should leverage data and insights to enhance quality management, transitioning to structured data for better analysis and continuous improvement. This proactive approach includes quick identification of root causes and implementation of corrective actions to prevent recurring errors. ⚗️Overall, a CDMO’s ability to meet quality expectations hinges on their commitment to continuous improvement and a culture that demands excellence. #pharmaceuticals #cdmo #researchanddevelopment #pharmaceuticalmanufacturing #apidevelopment #pharmaindustry #drugdiscovery #smallmolecule #cmcs #chemistrythatmatters #PharmaCDMO #drugdevelopment #contractmanufacturing #CMOservices #pharmasupplychain

💡 Do you know bioMérieux's 3P® ENTERPRISE solution for automated Environmental Monitoring?  Bridging the gap between standard processes and automation, 3P® ENTERPRISE revolutionizes the future of EM in the pharmaceutical industry. From sampling to trending, take control with an end-to-end, fully digitalized and automated workflow.  ⏱️ Gain time through faster reactivity ✅ Reduce risk of errors, deviations, and investigations 🔎 Be audit ready at anytime 🔄 Ensure maximum uptime

💡 Do you know bioMérieux's 3P® ENTERPRISE solution for automated Environmental Monitoring?  Bridging the gap between standard processes and automation, 3P® ENTERPRISE revolutionizes the future of EM in the pharmaceutical industry. From sampling to trending, take control with an end-to-end, fully digitalized and automated workflow.  ⏱️ Gain time through faster reactivity ✅ Reduce risk of errors, deviations, and investigations 🔎 Be audit ready at anytime 🔄 Ensure maximum uptime

💡 Do you know bioMérieux's 3P® ENTERPRISE solution for automated Environmental Monitoring?  Bridging the gap between standard processes and automation, 3P® ENTERPRISE revolutionizes the future of EM in the pharmaceutical industry. From sampling to trending, take control with an end-to-end, fully digitalized and automated workflow.  ⏱️ Gain time through faster reactivity ✅ Reduce risk of errors, deviations, and investigations 🔎 Be audit ready at anytime 🔄 Ensure maximum uptime