White Papers
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Validated LC–MS/MS Method For The Determination Of Copanlisib
11/14/2022
Review study findings on a validated LC–MS/MS method for quantifying copanlisib from a mouse dried blood spot and its potential for enabling desirable sensitivity, accuracy, and precision.
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Expediting Early-Phase Development Of Small Molecules: An Integrated Approach
11/1/2022
Small molecule APIs and drug products are more complex and potent than ever. Explore key strategies for efficiently advancing small molecules from API to pre-clinical data and clinical supply.
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Serialization And Traceability Compliance In Pharma And Med Device
10/28/2022
Explore the role of traceability and serialization and the benefits they offer beyond compliance. Further, gain perspective on how to approach UDI implementation and choose an appropriate solution.
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Key Considerations In Large-Molecule Orphan Drug Development
10/26/2022
Explore guidance for overcoming challenges with orphan drugs and ensuring that enough high-quality data is generated from the start of your program to guide evidence-based decision making.
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How Secure Is the Cloud for Pharma Manufacturers?
10/17/2022
Explore if the cloud is secure for pharma manufacturing and if the technology can really deliver on its promise to streamline operations.
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Eliminating Data Integrity Errors Through Digitization
10/17/2022
Explore the urgent need for businesses to adopt strong data integrity practices and identifies measures for how to achieve and sustain compliance.
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Five Biggest Considerations When Choosing A Buffer Management Solution
10/12/2022
Learn the five most significant considerations when choosing a buffer management solution that will aid manufacturers trying to decide which is suitable for their unique circumstances.
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Product D-Value Study - Part 2, Heat-Sensitive & Atypical Aqueous Liquids
10/5/2022
How can your organization use this critical tool when developing your sterilization process for heat-sensitive products and low F0 cycles?
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Why Perform A Product D-Value Study?
10/5/2022
Follow our discussion on non-heat sensitive aqueous liquid product sterilization and the use of the Overkill method and Bioburden/BI method.
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Product D-Value Studies: A Critical Tool In Sterilization Process Development
10/5/2022
Learn what questions to ask when developing a sterilization method and the critical tool that can help guide your decisions.