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Nipro April 2026
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Annex 1, Sterility Assurance, and the Rising Bar for PUPSIT

The latest revision of EU GMP Annex 1 has transformed sterile manufacturing expectations from a primarily reactive, end-of-line mindset into a fully integrated a...
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Why You Can’t Design a Prefilled Syringe System Out of Components

Over decades, the challenges of drug delivery have continually been met with innovation. Problems have been met with solutions. Take the prefillable syringe....
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The Platform Effect: Elevating Manufacturing Efficiency in Injectable Drug Delivery

“At its core, fill-finish involves taking a bulk pharmaceutical product – whether a vaccine, biologic, or small molecule – and precisely filling it into its fina...
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Automated Liquid Handling to Advance 3D Cell Culture

3D cell culture technology is rapidly gaining traction in drug discovery workflows, in particular for in vitro testing and simulation of disease progression and ...
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Xenotransplantation: Regulatory and Ethical Considerations with Best Practices for Sponsors and IRBs

Xenotransplantation, the use of animal organs in human recipients offers a possible solution to organ shortages but faces notable scientific, ethical, and regula...
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Multiplex Antibody Array Technology: Advantages and Applications

Proteins are involved in a wide array of biological processes, from apoptosis to cellular checkpoints and inflammation, among others, all of which are pertinent ...
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