Tilo Karschunke

Are you in the early stages of product development for an injectable drug? Then you won't want to miss our latest video featuring Jörg Zimmermann, Pharmacist and Vice President External Affairs at Vetter. 
 In this informative video, Jörg shares his top 5 tips on how to select the right primary container for your injectable drug product. He discusses the various factors that need to be considered when exploring container options beyond vials, including patients' evolving needs, the optimal container, injection device plans, import-export regulations, and deviation from standard components. Don't miss out on this valuable information that could make all the difference in the success of your product development. Check out our video now! #pharmaceuticals #productdevelopment #injectabledrugs #containers #expertadvice

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The FDA has specific requirements for labeling medical devices. Ensure your product meets all standards with our regulatory support. https://Vigilarebp.com #medicaldevices #didyouknow #vigilarebp #vigilare #Vigilarebiopharma #regulatory #fda #labeling #medical #devices #regulatoryaffairs

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Do you know what you need to consider before choosing a vial for drug development? Here are 5 things to help you get started. Read the full article here: https://lnkd.in/eNggc_xd SCHOTT Pharma West Pharmaceutical Services #pharma #pharmaindustry #drugdevelopment #vials #biotech #drugdiscovery #scienceparks #parenteralpackaging #drugformulation

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🕵️ Did you recognize him in our riddle? He was hiding behind the number 2 and is Director Health & Medical Technologies at Messe Düsseldorf GmbH. We're talking about Christian Grosser, of course. What he does during #MEDICA2024 and what a normal day looks like for him? 👉 Find out in the video!

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In healthcare and pharmaceuticals, sterile packaging plays a critical role in maintaining the safety and effectiveness of medical devices, instruments, drugs, and other products. The specialized process prevents contamination and ensures that the product remains sterile throughout its shelf life and during handling until usage. Read more about the processes, essential components, and applications of sterile packaging in our blog. #sterilepackaging #safety #contamination #sterile #healthcare #pharmaceuticals

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With copious amounts of data on your hands, your #pharma business faces big challenges and opportunities with it. A key factor? Your IT! Discover how High-Performance Computing technology can accelerate your R&D efforts: https://lnkd.in/eGe9Q5ei #pharmaceuticals #biotech

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🌍 Achieving CO₂ Neutrality in Pharmaceutical Production: Journey, Milestones, and Challenges Kicking off Day Two of the summit, Ulrich Schmöe, Global Engineering Director at NextPharma, presented on "Achieving CO₂ Neutrality in Pharmaceutical Production: Journey, Milestones, and Challenges." Ulrich provided an in-depth look into NextPharma’s company-wide project, sharing insights on: • The strategic approach taken to reach CO₂ neutrality • Key steps and milestones achieved along the way • The actions implemented to meet sustainability targets in a dynamic environment Thank you, Ulrich, for sharing NextPharma's inspiring journey toward a sustainable future! #NetZeroLifeSciences #Sustainability #CO2Neutrality #Pharma #NextPharma #LifeSciences #SustainableProduction

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Ensuring the integrity of container closures is crucial for the safe packaging of injectable drugs. Don't miss out—sign up for our webinar, Sealed for Safety: A Deep Dive into Container Closure Integrity, and discover how to evaluate CCI to guarantee the highest quality for injectable medications. https://bit.ly/3XNaKWx

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Ensuring the integrity of container closures is crucial for the safe packaging of injectable drugs. Don't miss out—sign up for our webinar, Sealed for Safety: A Deep Dive into Container Closure Integrity, and discover how to evaluate CCI to guarantee the highest quality for injectable medications. https://bit.ly/3zkW9Zb

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AVOID MANUFACTURING ERRORS WITH THESE 5 KEY QUESTIONS When an error occurs in pharma manufacturing, it's crucial to ask the right questions. This article by human performance/error prevention expert Sarah Boynton, MBA highlights five essential questions to understand and prevent such issues: What happened? What should have happened? Why did it happen? How can we prevent it? What lessons can we share? These steps help find the root cause and prevent future problems. Take a few minutes to read through the article for the deeper insights behind each question. Learn more about how to improve your processes, and let us help you achieve long-term success with our sustainable solutions: https://lnkd.in/evTF-PVu #pharma #biotech #qualityassurance

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Pharmaceutical News Review - September 2024 New interstate standards for specialists in the field of medicine and health care have been approved By the order of Rosstandart of September 3, 2024 № 1163-st the interstate standard GOST ISO/TS 37137-1-2024 “. The standard establishes requirements for assessing the biological effect of medical devices in the biological risk assessment process based on ISO 10993-1. The standard provides explanations of the terms “absorb”, “degrade” and other related terms (see Annex A). GOST ISO/TS 37137-1-2024 is introduced in the Russian Federation from March 1, 2025. GOST ISO/TR 21582-2024 “Medical devices. Evaluation of biological effect of medical devices. Principles and methods of research on pyrogenicity” was approved by the order of Rosstandart of September 9, 2024 № 1188-st. The standard establishes the principles and methods of research on pyrogenicity of medical devices and their materials. GOST ISO/TR 21582-2024 comes into effect in the territory of the Russian Federation from March 1, 2025. Read more: https://lnkd.in/gMSyEzy6

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Discover how Takeda Pharmaceutical leveraged Minitab's #PredictiveAnalytics Module to enhance production efficiency and increase yields for blood clotting drugs. Read this insightful #CaseStudy to learn more about their data-driven approach here: https://lnkd.in/gTHN9Yfj

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Does a #LearningManagementSystem Maximize Efficiency? In the pharmaceutical manufacturing industry, tackling skill gaps and providing targeted #training are key challenges. Learn how a robust #LMS can transform workforce development, ensuring compliance, safety, and product quality. Discover #QEdge's cutting-edge solutions designed for pharma! Click here- https://qedge.sarjen.com/ #TMS #TrainingManagementSystem #LMS #SarjenSystems #TrainingChallenges #Workforce #Pharma #PharmaManufacturing

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Pharmaceutical packaging lines have evolved into sophisticated systems that combine cutting-edge technology and proven methodologies to ensure safe, efficient, and compliant drug packaging. From automated filling and aseptic systems to advanced quality control measures, today’s packaging lines are designed for precision, cleanliness, and flexibility. With innovations like AI-driven inspection, robotic handling, and modular designs, these systems enhance production efficiency while minimizing contamination risks. Learn more about how modern packaging lines are shaping the future of pharmaceutical manufacturing. Read the full article below! #PharmaceuticalPackaging #Automation #AIinPharma #PharmaTech #Chemtech #IndustryInnovation

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