Search results for " analytical"

Article Essentials in Quality Risk Management
…phase during drug development and manufacturing and changes in drug-product formulation, definition, analytical method, and associated process changes are understood and managed to ensure patient saf…

Article The Importance of Partnering for Bioanalytical Studies
Depending on the type of assay, certain parameters may be added or removed to meet the assays’ context-of-use, and the analytical acceptance criteria may also vary. For immunogenicity assays, a statis…

Article Maximizing the Effectiveness of Upstream Bioprocessing Through the Combination of Lab Informatics and Instrumentation
Advances in analytical instruments are one key part of the solution. Novel techniques including Raman spectroscopy and other advanced monitoring methods have the potential to reduce the reliance on di…

Article Methods Accelerate Biosimilar Analysis
In May 2019, FDA published a draft guidance on the analytical assessment and other quality-related considerations for biosimilars, clarifying regulatory requirements and expectations for demonstration…

Article Evaluating E&L Studies for Single-Use Systems
• Many artifacts and analytical interferences were generated by strong/reactive solutions (as NaOH/NaClO), causing difficulties in the analyses and data interpretation; the use of strong saline/reacti…

Article A Platform Approach for the Identity Testing of Multi-Component Cell-Culture Media
The developed testing algorithm, which incorporates a combination of few relatively simple analytical methods such as osmolality, quantitation of glucose, and folic acid, provides specific identity co…

Article Virus-like Particles as Therapeutic Moieties of the Future
In this 44th article in the “Elements of Biopharmaceutical Production” series, the authors review the status of VLPs as therapeutics as well as challenges associated with their analytical and function…

Article Managing Residual Impurities During Downstream Processing
Increased understanding of potential impurities and their consequence to the ultimate quality, safety, and efficacy of biopharmaceuticals--as well as improvements in analytical technology that provide…

Article Witnessing Major Growth in Next-Generation Antibodies
Additional analytical and regulatory demands Next-generation antibodies also have their own set of analytical and regulatory challenges. With respect to analytical methods, each format/target comb…

Article Improving PAT for Biologics
Dec 01, 2014 By Cynthia Challener, PhD BioPharm International A key component of the quality-by-design (QbD) approach to pharmaceutical manufacturing is the implementation of process ana…

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