Gavin Statham MIHEEM MCIBSE’s Post

🔒 Closed Processing in Pharma 🔒 Sealed environments like isolators and containment systems keep both products and operators safe. ✅ Tightly controlled temperature, humidity, and pressure ✅ Automation minimizes human intervention, reducing contamination risks ✅ Perfect for aseptic processing and handling highly potent APIs 🔬 By embracing closed processing, we’re taking contamination control to the next level. 🌟 #Pharma #AsepticProcessing #ContaminationControl #ClosedProcessing #PharmaceuticalManufacturing #Automation #SterileManufacturing

Dear Pharma Professionals, Are you confident that your current cleaning agent effectively removes the toughest process residues, delivers consistent, validated performance, and is safe for both equipment and surfaces? Look no further – STERIS CIP 100 is the solution you need! 🔹 Superior Cleaning Power – Handles the most challenging residues 🔹 Validated Performance – Proven reliability across processes 🔹 Equipment & Surface Safe – Ensures longevity and compatibility 🔹 Globally Trusted – Compliance with international standards #PharmaCleaning #Biotech #CIP100 #ProcessSafety #CleaningValidation #CleanroomCompliance #PharmaceuticalSolutions #ProcessCleaning #AlkalineCleaner

Quality is not an act, it is a habit." - Aristotle We are no strangers to the importance of quality. We understand that one small mistake can have disastrous consequences, not only for our company but also for the health and well-being of our consumers. But what about the cost of quality? Are we doing enough to prevent it? Here are the things to think about:  ✅ Prevention  ✅Continuous Improvement  ✅Optimizations  ✅Technology  ✅Monitoring and Improvement #CostOfQuality #PharmaIndustry #Biotech #Manufacturing #QualityAssurance #BioCleaning #Business 👋Hi I'm Luis! 👋    I help Pharmaceutical and Biotech companies by working closely with the client to develop and document a Contamination Control Strategy (CCS), Cleaning Validation Framework and Strategies by using a framework that is process-driven and practical. This helps clients take control of their Cleaning Validation and Facility Cleaning.     ✔️ Join our monthly live online presentation for free, leave me a message to save your seat  

Exciting News Alert! Dive into our latest article focused on Facility Design Considerations for Hazardous Drug Compounding. Whether you're setting up a new facility or looking to optimize your existing one, this article addresses common questions and concerns! Visit our website for more information regarding consulting services and click the link to explore article now: https://bit.ly/44l7a7W #usp800 #hazardousdrugs #consulting #USP800consulting

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/eaZhdPm6

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/eStNyCYf

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

Great read if you work in life sciences, health care, or pharma. This report covers how to ensure compliance with the latest Ethylene Oxide (EtO) standards across your entire supply chain. https://okt.to/3ze2q9 #HealthCare #LifeSciences #Pharma #SupplyChain

Join us at the Cleaning Process & Validation Conference for a deep dive into the most crucial topics in pharmaceutical cleaning processes. 🔥 This impressive lineup of speakers and topics ensures a comprehensive understanding of the latest advancements and strategies in cleaning validation. Don't miss the opportunity to enhance your expertise and network with industry leaders. 📅 November 7-8, 2024 📍 Munich, Germany & Online 📑 Request full agenda: https://lnkd.in/da4z3R6h Day 2 Topics: ✔ASTM E55.11 Clean by Design: Richard Hall Hall from Rattiinox S.r.l. will introduce holistic strategies to enhance cleanability and operational efficiency. ✔Contamination Control Strategy: Dr. David Vincent, from VTI Life Sciences will provide an overview of contamination control plans and hygiene in cleanrooms. ✔Annex 1 and COP Machines: Fabio Buscaglia from IWT Pharma will discuss the latest on regulatory updates and where we are at Clean Out of Place machines. ✔Permitted Daily Exposures (PDEs): Dr. Martin Kohan, from Trinity Consultants - SafeBridge Europe, Limited will delve into calculating PDEs and their role in cleaning validation. ✔Flexible Single-Use Containment Systems: David Val from ILC Dover will explore the benefits of disposable containment solutions in meeting regulatory standards. Speak Pharma #SpeakCleaning #CleaningValidation #PharmaHygiene #IndustrionHygiene #CIPAdvantages #RiskAssessment #ManufacturingQuality #ValidationStrategies #PracticalApplications #CollaborativeLearning #QA #Digitalization #CleanByDesign #CIP #COP #Annex