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Articles by Dec Group
Dec Group Launches DecFill® XP
Ecublens, Switzerland – Dec Group has introduced DecFill® XP, a next-generation aseptic filling platform engineered to set a new benchmark for compact design, sustainability, and operational reliability in fill-finish manufacturing. As regulatory expectations tighten under EU GMP Annex 1 and manufacturers pursue smaller, more sustainable facilities, aseptic production platforms must deliver higher output with reduced complexity.
Dec Group brings game-changing RHEOFREED® to pharmaceutical freeze-drying
Ecublens, Switzerland – World-leading materials handling and process specialist Dec Group has launched RHEOFREED®, a revolutionary mixer-type freeze dryer that represents a breakthrough in continuous lyophilization technology. First unveiled at CPHI Worldwide in Frankfurt in October 2025, RHEOFREED® has now been formally added to Dec’s industry-leading portfolio following the establishment of a strategic partnership with Kobelco Eco Solutions of Japan.
Extract Technology Announces Full Integration into Dec Group
Huddersfield, UK — Extract Technology, a leading provider of containment and aseptic systems, is proud to announce its full integration into Dec Group, a global leader for integrated process solutions, serving industries such as Pharmaceutical, Biopharma, Nuclear & Chemical. This milestone marks the next phase in a successful partnership that began with Dec Group’s acquisition of Extract Technology in 2021.
Imagine a World
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01.23.26 -- A Deeper Look At Pharma's Structural Supply Chain Vulnerability
Pharma 4.0 in Action: Building Digitally Connected Packaging Operations with Open Standards Pharmaceutical manufacturers need faster, smarter, and fully compliant processes. This webinar shows how to connect shopfloor operations (OT) with enterprise IT for seamless machine integration, real-time data flow, and regulatory compliance. Körber experts share modular automation strategies for Pharma 4.0 readiness, explain OPC UA and PackML standards, and demonstrate Körber’s Line Optimizer live.
Will high containment solutions move towards standardized modular formats
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Dec Group showcases next-generation pharma manufacturing solutions at CPHI 2025 Frankfurt
Ecublens, Switzerland: – World-leading materials handling and process specialist Dec Group will use CPHI Worldwide 2025 in Frankfurt to demonstrate how global partnerships are driving new standards in pharmaceutical manufacturing – advancing innovation, sustainability, and performance. The Dec Group stand at Booth A10 will form a highlight of the Pharma Machinery and Equipment (P-MEC) Zone in Hall 9 of the Messe Frankfurt Expo Center.
Annex 1 and strategies for high-potency therapies
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What does the modern approach to high-potent APIs look like?
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Is micronization a bottleneck in formulation & process flow?
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How does modularity enhance process integration in OSD Manufacturing?
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Why does continuous manufacturing still feel like a leap for so many companies?
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From Powders to Precision - The Dec Journey
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Containment, more than a safety protocol
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DecFill® STU Sterilization Tunnel
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01.30.25 -- Here's Why The Life Sciences Struggle To Exploit Process Knowledge
A Closer Look At Inspection Systems In Tablet And Capsule Production Walk through the rigorous inspection process pharmaceutical products undergo to ensure safety and quality, from granulated ingredients to packaging. Considerations In Selecting A Biomaterial For Implantable Smart Devices Smart implants revolutionize healthcare with embedded sensors for real-time monitoring. Polycarbonate urethanes offer biocompatibility, overcoming challenges with biomaterials for safer devices.
10.31.24 -- Life Sciences Cybersecurity Incident Management: The End-to-End Approach
Revolutionizing Contract Manufacturing with a Unified QMS and MES Platform In the highly regulated life sciences industry, contract manufacturers face the dual challenge of ensuring product quality while maintaining efficiency across diverse production lines. Register to attend MasterControl's November 4th webinar to learn how QMS and MES integration enhances real-time decision-making, compliance, and product consistency—critical for meeting regulatory standards and safety requirements.
07.30.24 -- Making Good Decisions When FDA Investigators Come Knocking
Proactive Strategies To Evaluate And Mitigate Supply Risk Explore strategies that can help build an understanding of risk assessment, in addition to how to identify and address a study’s protocol requirements, drug characteristics, packaging specifications, and more. Understanding Biosafety Levels To Ensure Safety Compliance with biosafety levels (BSLs) is crucial in ensuring that your laboratories meet stringent standards to protect staff and prevent the escape of biological agents.
02.09.24 -- Driving Pharma/Biotech Capacity With Smart Manufacturing
It's time for manufacturers to consider a new approach to capacity management, one that can not only resolve today’s challenges but also position the enterprise to drive innovation and resilience in the future. You can leverage a smart manufacturing approach in three vital ways. Media And Feed Development: A Guide To Workflow Optimization Gain insight into each development stage and explore best practices that will help achieve your project goals on time and within budget.
Erreichen Sie ein neues Maß an Produktivität und Exzellenz
80 % der Prozesse in der chemischen Industrie sind mehrphasig. Typische zweiphasige Flüssig-Flüssig-Reaktionen erfordern eine hohe Wärmeübertragungsfläche pro Einheitsvolumen. Dec bietet vollautomatische Prozesslösungen für homogene und mehrphasige Prozesse im kontinuierlichen Betrieb an. Prozesse in der chemischen Industrie werden zu etwa 80 % als Mehrphasen-Prozesse durchgeführt, beispielsweise Fest-Flüssig, Flüssig-Flüssig, Gas-Flüssig und Fest-Gas-Flüssig.
Keeping it contained: How the industry is evolving?
The containment industry is evolving – are you? Asks the Dec Group Realising the desired levels of containment to minimise operator exposure while protecting sterile products is a complex process in which nothing can be left to chance. Aseptic high-potency API processing calls for specialised facility design to help pharma improve and maintain the sterility of its drug products.
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