Insights On Facility Design
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Multiple Fill Line Delivery Experience
8/16/2025
Learn how a multinational pharmaceutical company successfully implemented a global strategy for insulin cartridge filling, achieving seamless regulatory approval with zero deviations.
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Stories From The Field: Supporting Critical Steps In Fill And Finish
8/7/2025
Explore the critical final step in drug development—formulation and filling—and discover expert strategies that can help streamline operations, reduce risk, and enhance efficiency.
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A Contamination-Reducing Solution In Aseptic Transfer
8/7/2025
Discover a technology that delivers a validated, contamination-reducing solution for sterile component transfer in aseptic environments to streamline operations under Open RABS with glove-free handling.
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Normalized Data In Microbial Continuous Monitoring
7/24/2025
Learn how EU GMP Annex 1 (2022) redefines cleanroom air monitoring standards and emphasizes continuous viable sampling in Grade A and B environments to ensure aseptic integrity and compliance.
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Sustainable Vaccine Manufacturing: Securing The Future Of Global Health
7/22/2025
Explore how next-gen technologies, from mRNA platforms to digital tools, are transforming vaccine manufacturing to make it more sustainable, flexible, and accessible.
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Using Algae To Manufacture Oral Biologics With Lumen Bioscience's Craig Behnke, Ph.D.
7/15/2025
Lumen Bioscience is putting the farm in biopharma — literally! In this episode of Better Biopharma, Lumen's EVP of production and development, Craig Behnke, Ph.D., explains the company's chlorophyll-powered approach to bioprocessing using photosynthetic cyanobacteria.
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A State-Of-The-Art Syringe Liquid Sampler
6/24/2025
Discover a cutting-edge syringe liquid sampler for Life Sciences that offers USP <788> compliance, versatile syringe compatibility, and advanced features for precise particulate testing.
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Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations Part 2
6/16/2025
Learn essential conceptual design principles for transforming alternative spaces into efficient, regulatory-aligned cleanroom environments for your critical processes.
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How A Rigorous Approach Delivers Unparalleled Results
6/12/2025
In critical environments where mistakes have serious consequences, a disciplined, methodical approach isn't just a preference—it's the only path to success and long-term operational excellence.
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Revolutionizing Pharma Validation With AI
5/28/2025
Validation in GxP environments is often the bottleneck in digital transformation—manual, repetitive, and complex. One company's Intelligent Agents are transforming that process.