Meet our skilled lab technician, adept at blending a wide range of ingredients to create both basic and groundbreaking drug formulations. The mixing process is a crucial step in the development of drug formulations, ensuring that the final product has a consistent appearance and quality, guaranteeing uniform content throughout. Curious to know how we can support your formulation needs? http://ms.spr.ly/6041lv5Kh
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🔬 Elevate Your COD Testing with #CODReactor! "Compliance with regulations" just got easier! The WD325 simplifies your COD testing process with innovative features: ✅ Regulatory Compliance: Meets USEPA 410.4 standards, providing safer and more efficient digestion compared to traditional methods. 🚀 Special COD Program: Press start, and the reactor heats to 150°C for a 2-hour countdown, automatically shutting down with an audio alert. ⚙️ Customizable Settings: Set temperature between 60°C - 200°C, and timer from 1 - 999 minutes, with 3 built-in programs for flexible testing. 🔔 Auto Shut Off & Alarm: Never worry—WD325 stops heating and shuts off with an audio alarm when done! Enhance your lab's performance today! 🔗 Learn more...! visit: https://lnkd.in/d4J9C4Ht for queries, write to us at info@srico-labworld.com or call us at +91 9900674407. #srico #wiggens #labequipment #laboraotryequipment #pharma #pharmaceutical #pharmamanufacturing #rnd #science #qualitycontrol #Qc #chemicalindustry #Pharmaceuticalmanufacturing #petrochemicalindustry #automobileindustry #researchanddevelopment #research #LabEquipment #Innovation #Quality #Sustainability
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📢 Here's your reminder to sign up for our webinar with #Recipharma on January 25 before it's too late 📢 During this webinar, we will explore the possibilities offered by a phase-specific regulatory strategy for overcoming challenges associated with the CMC (Chemistry, Manufacturing, and Controls) approach for ATMPs. Register for free below! https://bit.ly/476U1Ql
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#First-in-human trials are crucial as they provide sponsors the opportunity to evaluate the safety and efficacy of their #investigationalmedicinalproduct in human subjects, laying the foundation for subsequent clinical phases. However, the process of writing comprehensive chemistry, manufacturing, and controls dossier modules to support these studies can be complex, demanding meticulous attention to detail and adherence to regulatory guidelines. Our checklist serves as a roadmap for #biotech and #pharma companies undertaking this process, helping them generate all the paperwork required to advance their novel treatments to the next stage of the development lifecycle. Get it here: http://spr.ly/6040bR7v0
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This is my first webinar with Recipharm. Looking forward to discussing ATMP stability topics with you next week!
As you prepare to bring your ATMP product to market, you face a range of challenges across the Chemistry, Manufacturing, and Controls (CMC) processes along the way. In our upcoming webinar, our experts Melanie Cerullo M.S., CQA, Chief Quality and Regulatory Officer and Joseph Bibeault, M.S., Director, Regulatory CMC, will share their insights and advice on how a phase-specific approach can help you overcome your CMC challenges while saving time and reducing costs. Sign up below to secure your place: https://lnkd.in/d3T8STpn #ATMPs #CMC #DrugManufacturing #PharmaWebinar
ATMPs in Focus: Essential CMC Strategies for Every Phase
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Microbiological Safety Cabinets (MSC), also known as Biological Safety Cabinets (BSC), are the unsung heroes of biotech, pharmaceutical, and clinical labs! These ventilated enclosures are crucial for maintaining a safe and sterile environment during your experiments. There are three main types of MSCs: Class 1 Class 2 Class 3 But here's something every lab tech should know: According to COSHH Regulations, these cabinets need regular check-ups to ensure they’re working perfectly! The inspection schedule is as follows: - For Containment Level 1 (CL1) work: Annually - For Containment Level 2 (CL2) work: Every 6 months (advisory) - For Containment Level 3 (CL3) work: Every 6 months (mandatory) Stay safe and keep your lab in top shape by staying on top of these maintenance intervals. Get in touch with the team to book in: Tel: 01257 262 683 Email: sales@rjurmson.com #LabSafety #Biotech #Pharma #ClinicalLab #SafetyFirst
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Your custom batch release journey explained! Batch release refers to the process of evaluating and authorising a specific batch of a drug product to ensure it meets all required quality standards before it is released for distribution. At HMR Labs, our custom journey includes: Defining your requirements ⬇️ Initial consultation with the scientific team ⬇️ Strategy development and testing plan ⬇️ Validate testing methods alongside regulations Establish validated methods within our laboratories ⬇️ Devise sampling plan protocols ⬇️ Data generation for release decision making Trust us to guide you through every step of the batch release process with precision and expertise. Discover more: https://bit.ly/3MelAP2 #pharmaceuticalindustry #qualityassurance
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🔬 Optimize Your Filtration Processes with a Filterability Study from Meissner! Achieving the best process performance and product quality starts with selecting the right filter. With countless options on the market, Meissner offers expert guidance to help you make the pore-fect choice. What do our Filterability Studies typically entail? Tailored Solutions: 🧪 Our team of scientists perform scale-up tests with your product using disc filters to evaluate various filter options, helping us determine the ideal size, type, and number of filters for your specific process. Efficiency Improvements: 🚀 We ensure precise filter sizing, eliminating unnecessary oversizing to enhance efficiency. Data-Driven Insights: 📊 Get detailed performance reports and side-by-side membrane comparisons to find the most efficient and effective filter for your needs. Expert Support: 🤝 Receive personalized consultation and technical assistance from our team of seasoned filtration specialists. Discover how our Filterability Studies can elevate your biopharma processes. Learn more about our services by visiting https://lnkd.in/gHjncmJR or request a consultation by reaching out to me at luke.hanson@meissner.com. #Biopharma #FiltrationSolutions #FilterabilityStudies #Meissner #LifeSciences #Pharmaceuticals #Biotech #FilterTechnology #ProcessOptimization
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Take the chance to learn more about #SprayDriedDispersions!
A well-understood risk-based manufacturing process in drug development is critical to success. From support process qualification for amorphous solid dispersions by spray drying to process validation strategies and small-scale experimentation – our latest webinar is designed to guide industry directors, CMC leads, development engineers and technical operators toward better development outcomes. Join us on Thursday, June 20, 11:00am EDT to discover the commercial capabilities of using a CDMO, the essential attributes of SDD formulations, and how to achieve reduced risk and material use. To register your place, visit: https://lnkd.in/dAM4k_Qe #LonzaSM #WeWorkAsOne
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CALIBRATION OF VOLUMETRIC GRASSWARES In the world of pharmaceuticals 💊⛑️, precision is super important – where every drop 💧 counts. Imagine a scenario where knowing the exact volume of a liquid becomes really crucial. That's why calibrating glassware 🧪👩🔬 is not just something we do; it's something we absolutely need ☑️ In the heart of laboratories, chemists use a careful process to make sure that our glasswares are accurate. #Glassware is commonly calibrated using a liquid of known, specific density, and an analytical balance. The procedure is to determine the mass of liquid the glassware will hold which is the important part of calibration process. Now, armed with the mass and the known density of the liquid, chemists do some math. They divide the measured mass by the density, finding out the actual volume that the glassware can hold. This isn't just a technical step; it's like making sure that every measurement taken with that glassware is super accurate. So, the next time you see a chemist calibrating glassware in a pharmaceutical lab, remember it's not just about numbers – it's about making sure that every drop in the pharmaceutical world is measured with the most accurate info. Calibration, basically, is the quiet hero behind the scenes, making sure that science moves forward with super exact measurements. What more insights can you share about the calibration of glassware? 🧪✨ After knowing the actual volume what next?? which liquid is used in calibration of glasswares and why?? is temperature of liquid matter?? and the density?? where does it comes from😉?? let's share knowledge #GlasswareCalibration #PrecisionInPharma #LabLife #LabAccuracy #ChemistryEssentials #CalibrationMatters #ScientificPrecision #Pharmaceuticals #GlasswareCalibrationTips #QualityControl #LabProcedures
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Dive into the world of Quality with our latest blog post! Explore the critical Quality components within Modules 2 and 3 of the eCTD. From the Quality Overall Summary to detailed insights on drug substance and product, learn about what is included. This is a quick overview for people who want to know more about the Quality aspects of an application without requiring a Chemistry background. https://lnkd.in/eZbH3AQt #eCTD #Quality #regulatorysubmissions #submissionready #regulatoryoperations
What are the Quality (CMC) Components of the eCTD?
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