INSIGHTS ON PHARMACEUTICAL LOGISTICS
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Optimized Processes: A Guide To Lyophilization Cycle Development
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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Cryogenic Storage Of IV Bags For Cell And Gene Therapies
Cryogenic storage can compromise packaging integrity for cell and gene therapies. Learn how vacuum decay technology detects micro leaks and ensures product safety under extreme conditions.
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Outsourcing To ISO 17025 Accredited Suppliers
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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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?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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Building A Purification Toolkit For An Expanding Variety Of mAb Therapeutics5/29/2025
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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Supply Resiliency For Bioprocessing Amid Global Volatility10/2/2025
Build bioprocessing resiliency with strategic supply chain management. Learn to meet quality, compliance, and time-to-market demands amid global volatility with effective sourcing.
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Strengthen Pharmaceutical Supply Chains With A U.S.-Based CDMO6/5/2025
While certain ingredients require sourcing abroad, partnering with a U.S.-based company that owns its manufacturing assets allows for direct oversight of product quality and supply reliability.
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Moving Batch Release Into The Fast Lane1/21/2026
Complex supply chains and fragmented systems slow batch release, delaying patient access and revenue goals. Learn how automation and centralized data improve compliance and accelerate delivery.
PHARMACEUTICAL LOGISTICS SOLUTIONS
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Sourcing NaCl solutions can help streamline your buffer preparation allowing you to focus on additional critical steps in your biopharmaceutical processes.
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V57- Customizable, precise quality control
Immediate contamination detection and precision formation inspections of rigid plastic containers.
Advanced Product Handling
Product tracking, product handling options, and intuitive software enable efficient visual inspection of every product.
Real Time Quality Control
Installed directly after product formation, the system minimizes chances that misformed or contaminated products continue to downstream processes.
Precise Package Presentation
Detect product contamination as small as 0.1 TAPPI for top-quality products.
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How your manufacturing, packaging, serialization, and clinical distribution can benefit with a contract partner.
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Learn how Vertiva™ can enable delivery of micro-precision basal doses and full-content bolus injections, resulting in a highly flexible, customizable platform suitable for a wide range of therapies.
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Easily blended in a child’s food or beverage, pediatric powders in unit-dose stick-packs provide taste masking and convenience without compromising integrity.