INSIGHTS ON PHARMACEUTICAL LOGISTICS
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Top Safety Considerations In Biopharmaceutical Manufacturing
Understanding top safety concerns, from combustible material handling and chemical exposure to HPAPIs, is the first step toward preventing accidents in biopharmaceutical manufacturing environments.
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Shedding Light On Photo-Stability Forced Degradation
Ensure the stability and safety of your drug products by utilizing comprehensive forced degradation and photo-stability testing, guided by ICH and FDA standards, to identify degradation pathways and assess light exposure risks.
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Supply Chain Efficiency And Sourcing In Gene Therapy
An overview of the inbound supply chain in gene therapy and the process development challenges that are frequently faced. Learn about concepts such as scaling, cell culture media sourcing, mixing technologies, and configurable packaging.
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Clinical, Commercial Packaging: Delivering Next-Gen Therapies
See how strategic, agile, and sustainable packaging is transforming drug delivery into a key driver of speed, safety, and patient-centric innovation.
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Windsor Framework: What Is It?9/2/2025
Learn about the Windsor Framework and how it addresses the challenges of medicine supply chains between the UK and the EU, creating stability and certainty in the post-Brexit world.
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Risk Mitigation For Late-Stage Clinical Assets6/11/2025
Leveraging the competence and capabilities of the CDMO to bring forth innovative, flexible solutions to safeguard supply chains for their clients and, ultimately, for patients is crucial to strategic partnering.
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The Future Of RNA Manufacturing Starts With Raw Material Innovation2/11/2026
Amid the mRNA and oligonucleotide therapeutic boom, sponsors and manufacturers are exploring how to make critical raw materials—capping agents, lipid nanoparticles, and RNA polymerase—more effective.
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Friendshoring: A Strategic Shift In Pharma Supply Chains4/11/2025
To safeguard the consistent delivery of essential therapies to patients around the world, biopharmaceutical companies, alongside their CDMO partners, are rethinking traditional supply models.
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Site Transfer Of Tablet Production From Ex-U.S. To Georgia Site6/11/2025
Explore how strategic U.S.-based manufacturing and supply chain diversification can reduce risk, lower costs, and enhance supply reliability for pharmaceutical products.
PHARMACEUTICAL LOGISTICS SOLUTIONS
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Used Cu ft Matcon IBC bin, stainless steel construction, approximately 43" x 43" x 15" straight side x 27" deep cone bottom, fork access and stackable, serial# 2298.
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How can you safely transport masses of delicate syringes along production lines at a speed that benefits your business? What about all your specific product requirements? Our cutting-edge overhead conveying, lane management, accumulator and buffer solutions are scalable and adaptable – and we handle all your products with care.
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When working in a critical environment such as a clean room or when producing critical bioproducts, even microscopic amounts of contamination can have a disastrous impact. The tiered portfolio of Thermo Scientific™ Nalgene™ containers provides bioproduction facilities with a range of high-quality sterile storage and transport options while addressing particulate level (USP <788>), endotoxin level, and sterility requirements
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SKU: 4486-17
Item Name: Qualicaps Capsule Bander, Model S-100
Category: Capsule Fillers/Encapsulators > Capsule Banding Equipment
Manufacturer: Qualicaps
Location: Cleveland, OH
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Used Farrar Trane Technologies Ultra Low Storage Chamber, Model ULC 259, 259 cu ft / 7334 liter total volume, -80 to +10 c temperature range, 73.2 sq ft chamber floor space, box capacity 3920 for 2" freezer boxes, 2520 for 3" freezer boxes, vial capacity at (81) vials/box 2" boxes 317,250 or 3" boxes 204,120, dual refigeration system with (4) total compessors, R449, R290 and R508B refrigerant, approximately 3073 mm wide x 1741 mm depth x 1741 mm high chamber dimensions, approximately 3381 mm wide x 1935 mm depth x 3234 mm exterior chamber dimensions with refrigersation sections.