Insights On Liquid Dose Manufacturing

1. Three Key Actions To Minimize Dead Volumes 10/10/2025

   Minimizing liquid dead volume helps labs conserve costly reagents and scarce samples while boosting assay throughput. Learn how advanced liquid level detection technologies are driving efficiency.

2. Compressed Gas Systems In Aseptic Manufacturing 10/18/2024

   Learn about compressed gas systems and why effectively identifying and managing the risks associated with these systems is critical for maintaining product quality and ensuring compliance with GMP.

3. Generate CHO-K1 GFP-Expressing Cells For Cell Line Development Workflow 11/7/2025

   Discover a high-efficiency workflow for generating GFP-expressing CHO-K1 clones using automated single-cell dispensing to achieve 93% isolation success and stable expression in under five weeks.

4. Ready-To-Use Cartridges: Ensuring Compatibility For GLP-1-Based Drugs 8/27/2024

   Ready-to-use cartridges for GLP-1 applications offer safe, reliable self-administration. See how they can minimize complexities and better align with the stringent demands of modern manufacturing.

5. Turnkey Dismantling, Modification, And Relocation Of A Multi-Glove Isolator System 1/30/2026

   Strategic equipment relocation and retrofitting can reduce capital costs by fifty percent and save months in lead time. Learn how to modernize legacy systems while maintaining full GMP compliance.

6. 5 Common Bowie-Dick Test Failures And How To Prevent Them 11/26/2025

   Bowie-Dick test failures indicate serious sterilization issues. Learn the five most common causes and proven strategies to prevent downtime, compliance risks, and compromised product integrity.

7. How Do We Reduce Your Environmental Cost Of Ownership (ECO)? 12/4/2025

   By rethinking cleanroom requirements and reducing resource-heavy sterilization steps, manufacturers can significantly lower their Environmental Cost of Ownership and futureproof their operations.

8. Accelerating Sterile Injectable Innovation Through Strategic Outsourcing 9/21/2025

   Sterile injectables are vital for modern medicine. Learn how outsourcing manufacturing to a CDMO can accelerate development and commercialization.

9. Consistent, Reliable, High-Quality Components 2/3/2026

   Discover a premium line of components for vials, prefilled syringes, and cartridge systems developed and refined to provide best-in-class levels of quality, performance, and risk mitigation.

10. Ensure Sterility In Small-Batch Drug Production 1/9/2026

    Automation and sterility are critical for small-batch drug manufacturing. Learn how robotic isolators streamline vial filling, reduce contamination risk, and support advanced therapies with precision.