INSIGHTS ON PHARMACEUTICAL LOGISTICS
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Building A Purification Toolkit For An Expanding Variety Of mAb Therapeutics
Explore techniques for optimizing purification toolkits for various monoclonal antibody formats. This session covers resin and buffer selection for efficient downstream process development.
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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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Windsor Framework: What Is It?
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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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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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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Embracing Digital Transformation In Life Science Manufacturing: A Path To Excellence1/13/2025
Discover how life science manufacturers are supported in digital transformation, offering solutions for automation, data integration, and compliance to optimize operations.
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Optimized Processes: A Guide To Lyophilization Cycle Development6/25/2024
Review the essential phases of the lyophilization cycle — freezing, primary drying, and secondary drying — and critical success factors to achieve optimal product quality and stability.
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Outsourcing To ISO 17025 Accredited Suppliers1/28/2025
Discover the advantages of outsourcing equipment calibration to ISO 17025 accredited suppliers, including cost efficiency and regulatory assurance, in our detailed analysis. Read more to transform your calibration processes.
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The Team For Your Package Design Needs8/16/2025
Our dedicated team of in-house design specialists deliver insightful packaging design and practical knowledge to deliver differentiated and cost-effective packaging solutions.
PHARMACEUTICAL LOGISTICS SOLUTIONS
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Our cutting-edge technology and impeccable standards ensure that our customers receive products that meet their exact needs.
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Ropack's portfolio of primary pharmaceutical packaging methods meets the highest quality and safety standards.
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V15 Label Inspection 360° System
Compact, efficient, and reliable. This space-saving solution detects label data and quality defects on round products. Six image sensors are enclosed in a compact design that can easily be installed over existing conveyors. The V15 can be extended with top and bottom cameras.
100% Automated Label Inspection 360°
This cost-effective vision system is ideally suited to replace manual spot checks with 100% automated label inspection control for round products.
Compliance Support
The V15 supports consumer safety in offering documented label inspection in line with industry guidelines such as IFS and BRCGS.
Reduce Waste and Prevent Recalls
The V15 verifies labels to detect and reliably sort non-conforming products to avoid costly recalls due to false or missing declarations.
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Used VWR ULT freezer, model 5706, capable of -80 C temperatures, R-404a, R-508b refrigerant, 2 stage operation, with chart recorder and controls, (4) shelves, 208/230 volts, serial# 833437-852, built 2013.
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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