Authors
Latest:
Achieving Intensification and Flexibility in Virus Purification with Next-Generation Chromatography ToolsThis article discusses the potential of using high-productivity membrane chromatography to achieve intensified and flexible virus manufacturing.
Latest:
Achieving Intensification and Flexibility in Virus Purification with Next-Generation Chromatography ToolsThis article discusses the potential of using high-productivity membrane chromatography to achieve intensified and flexible virus manufacturing.
Latest:
Achieving Intensification and Flexibility in Virus Purification with Next-Generation Chromatography ToolsThis article discusses the potential of using high-productivity membrane chromatography to achieve intensified and flexible virus manufacturing.
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Inside the Lab of the FutureDrive growth by establishing integrated, AI-fueled lab systems and a data-driven corporate culture that’s ready and resilient, no matter what business challenges emerge tomorrow. Evolving to a Lab of the Future takes the right technologies, systems, and expert guidance.
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A Three-Step Path Toward Combination Product ApprovalThis article describes how to improve the regulatory journey from classification to market clearance for sponsors of medical device combination products.
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Reliability Rooms and the Move to Proactive Supply Chain ManagementCross-functional reliability rooms identify risk and planning metrics, provide insights for production forecasts, and predict trends and areas for improvement.
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Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
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Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
Latest:
Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
Latest:
Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
Latest:
Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
Latest:
Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
Latest:
Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
Latest:
Approaches to USP OTC Monograph ModernizationThe authors hope to facilitate further collaboration among all the stakeholders for USP OTC Monograph Modernization with the goal of identifying a satisfactory approach for USP, FDA, and industry.
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Selecting a Specimen Holder for X-ray Powder DiffractionSpecimen mounting in x-ray powder diffraction affects peak positions and intensities.
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Selecting and Installing Peristaltic Pump TubingProper selection and installation optimizes fluid system performance.
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A Resurgence in Natural Product-Based Drug DiscoveryAdvances in analytical technology are making the screening of natural products and their substructures more viable.
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Using Labels to Detect and Prevent TamperingLabels must have special features to prevent tampering of pharmaceutical packaging.
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Applying Continuous-Flow Pasteurization and Sterilization ProcessesHigh-temperature, short-time (HTST) pasteurization and ultra-high temperature (UHT) sterilization are potentially useful as part of the trend toward methods of continuous manufacturing of bio/pharmaceuticals.
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Determination of Dermal PDE for Pharmaceutical ProductsThe authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
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Determination of Dermal PDE for Pharmaceutical ProductsThe authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
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Determination of Dermal PDE for Pharmaceutical ProductsThe authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
Latest:
Determination of Dermal PDE for Pharmaceutical ProductsThe authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
Latest:
Determination of Dermal PDE for Pharmaceutical ProductsThe authors offer recommendations for permissible daily exposures and concentration limits of elemental impurities for dermal drug products.
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How Particulate Modelling will Revolutionize the UK’s Pharmaceutical SectorParticulate modelling has the potential to transform productivity within the pharmaceutical manufacturing industry, speeding up production cycles, reducing manufacturing costs, improving efficiency, and driving inward investment, with the potential to reinstate the UK as a global manufacturing powerhouse.
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Removing Subjectivity from the Assessment of Critical Process Parameters and Their ImpactA new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
Latest:
Removing Subjectivity from the Assessment of Critical Process Parameters and Their ImpactA new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
Latest:
Removing Subjectivity from the Assessment of Critical Process Parameters and Their ImpactA new algorithm uses a statistical approach to critical process parameter assessment, allowing for faster, more consistent, and less subjective critical process parameter quantification, visualization, and documentation.
