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The author provides an overview of common residual moisture methods for lyophilized drug products and key points to consider during method selection and method development. MR.ILKIN/STOCK.ADOBE.COM ...
The quality of a lyophilized drug relies on a complex inter-play of the product, the process, and the container. Glass containers remain the gold standard for lyophilization, although ...
The lyophilized injectable market is poised for growth due to increasing demand for biologics and specialty drugs, R&D activities, and global collaborations. Key opportunities include leveraging ...
Lyophilization removes water to prevent degradation, ensuring the product remains potent and safe for use. Ease of transportation: Lyophilized drug products typically require non-frozen storage ...
The FDA is alerting health care providers, hospital supply managers, and pharmacists that sterile drug products compounded by ApotheCure, Inc. and sterile lyophilized drug products from NuVision ...
The in-use time is defined as the maximum amount of time that can be allowed to elapse between penetration of a container-closure system containing a sterile drug product, or after a lyophilized ...
The lyophilized injectable drugs market has seen a growing array ... reagents has also bolstered the demand for lyophilized products with high biological and chemical activity.
Dublin, Oct. 30, 2024 (GLOBE NEWSWIRE) -- The "Lyophilized Drugs, Reconstitution Devices and Injection Markets: Products, Markets, Therapeutics, Strategies & Forecasts" report has been added to ...
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