INSIGHTS ON QUALITY CONTROL
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High-Throughput Released N-Glycan Identification
Learn about an all-inclusive sample preparation and high-throughput glycan analysis workflow with a customizable molecule-specific glycan library.
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Enhance Peptide Innovation With A High-Quality Supply Of Building Blocks
To leverage the benefits of peptide therapeutics, identify an experienced chemical material manufacturer that can produce unique peptide building blocks with quality, efficiency, and continuous compliance.
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Innovative Technology For Developing, Scaling Peptide-Based Therapeutics
Watch as experts walk through several technologies and case studies, focusing on liquid-phase peptide synthesis, crystallization, method development for impurity analysis, and more.
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Leachables Method Development, Validation And Relevant ICH References
It is crucial to develop and validate analytical methods capable of detecting a wide range of potential organic and inorganic leachables specific to the drug and its packaging.
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Contamination Control Strategy With QRM Principles11/19/2024
Contamination Control Strategies (CCS) have long been a main concept, but advancing requirements and regulatory expectations create a challenge. Learn how to be effective and compliant with your CCS.
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Intro to USP <1062> — What Is Tabletability?7/20/2023
What is tabletability, and why is it important for creating tablets that can survive the journey from manufacturing to packaging?
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Seamlessly Integrating An E-WorkBook With A Customer's LIMS8/12/2024
Explore the story of a global biopharma company's integration of E-WorkBook with their LIMS, automating ADA study reports, saving significant time, and enhancing data accuracy.
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Filling The Sterility Testing Gap: Traceability And 21 CFR Part 11 Compliance6/6/2024
Watch to learn about a solution that offers digital information for every stage of a sterility test while remaining compliant with 21 CFR Part 11.
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Mitigate Human Error And Improve Performance In Pharma QC7/17/2023
Gain insight into how the Quality Control team at Almac Sciences developed processes and strategies to help ensure a high quality of safe and effective products while also maximizing efficiency.
QUALITY CONTROL SOLUTIONS
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Explore end-to-end solutions and products suited to your organization, whether for research and discovery or planning for scale to commercial manufacturing.
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Ensure your equipment meets stringent regulatory expectations with an instrument qualification service that supports you through installation, maintenance, and modifications for compliance.
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Discover a 21 CFR Part 11-compliant digital validation platform designed for conducting IQ & OQ on your microbial QC testing systems dedicated to bioburden testing, sterility testing, and air monitoring.
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The Powder Rheology Accessory expands the DHR’s capabilities to powders, enabling the characterization of behaviors during storage, dispensing, processing, and end-use.
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API Process Development System designed to provide personnel and product protection while working with powder and liquid substances. Designed to house a Mettler Toledo Easy Max 102, Vacuum Oven, and IKA LR 1000.