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| home > white papers > Value-Added Processing and Quality By Design Principles Help Meet High-Quality Demands - West Pharmaceutical Services, Inc. |
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 WHITE PAPERS |
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West Pharmaceutical Services, Inc.
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Value-Added Processing and Quality By Design Principles Help Meet High-Quality Demands
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The current pharmaceutical market has faced a variety of challenges,
including increasing expectations for quality from end-users and
regulatory agencies driven by concern for patient safety. While
pharmaceutical companies are working to assure that new quality and
compliance paradigms are met, a balance must be achieved between the
reality of managing costs in an effort to provide a product that meets
the requirements of payers along with facilitating profitability in
order to continue adequate business reinvestment.
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News and Press Releases |
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Protagen Protein Services (PPS) reaches new level in characterizing HCP protein impurities
In response to current regulatory guidance a Mass Spectrometry (MS)
based Host Cell Protein (HCP) detection approach with faster, more
accurate and wider-ranging detection is essential. In order to meet the
newly prevailing demands Protagen Protein Services (PPS) recently
invested in more far-reaching MS capabilities: The new high-performing
mass spectrometer ThermoFisher Q Exactive™ HF-X started operational
service last month and brings PPS to the next level of reproducible,
accurate and sensitive analyses of majorly complex samples for different
aspects of translational research and biopharma applications.
More info >> |
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White Papers |
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Recommendations Sourcing Human Biospecimens
BioIVT
The foundations for protecting human research subjects come from the
ethical principles surrounding the Belmont report : Respect for persons,
beneficence, and justice. The use of human biospecimens in research
supports these principles with legal and ethical regulations - the most
important of which is permission.(1) This permission may come directly
from the donor or granted by others with authorization to protect the
interests of biospecimen donors.
More info >> |
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Industry Events |
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Clinical Trial Supply Europe 2019
13-14 March 2019, Milan, Italy
Following
on from our largest and most engaging meeting to date, Clinical Trial Supply
Europe will be returning to Milan for its 20th year in 2019!
The
19th annual edition welcomed pharmaceutical companies across Europe who got
together to share knowledge and issues regarding clinical trial supplies, both
with regards to operational and technological challenges. Over the two days,
delegates discussed issues which affected their business in our dedicated
operational and technological streams.
More info >> |
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