MORE WATER INDUSTRY FEATURES

• LC-UV-Based Synthetic Peptide Impurity Tracking And Reporting

  Explore a UPLC-UV method using Empower 3 Software to assess synthetic peptide purity. Learn how integrated tools streamline impurity tracking, data reporting, and compliance in peptide analysis workflows.

• Development Of A High Sensitivity SPE-LC-MS/MS Assay

  Achieve ultra-sensitive glucagon quantification with ionKey/MS, μElution SPE, and advanced MS fragmentation to deliver low LOD, reduced sample loss, and enhanced confidence in results.

• Ozone And PFAS: The Overlooked Tool In A National Water Crisis

  Ozone is a vital pre-treatment for PFAS mitigation. It oxidizes precursors and co-contaminants, significantly extending the service life of downstream GAC and membrane systems.

• AMERICAN And Partners Install Boltless Restrained Underwater Pipeline System In Ashland, Wisconsin

  Beneath the waters of Chequamegon Bay on Lake Superior in Ashland, Wisconsin, about 4,500 feet of 24-inch AMERICAN Flex-Ring Ductile Iron Pipe and a submerged timber crib intake structure were installed to ensure the city’s residents have quality drinking water for the next 100 years. The Ashland Water Intake Project began May 1, 2025, and is now complete.

• Lentiviral Vector Upstream Process

  Scalable lentiviral vector production is moving beyond adherent systems. Learn how streamlined workflows enable linear scale-up in stirred-tank bioreactors for cost-effective gene therapy manufacturing.

• Optimizing TFF And SPTFF For High-Concentration mAb Formulations

  Discover the critical role of formulation buffer composition in stabilizing monoclonal antibodies during tangential flow filtration, a process involving ultrafiltration and diafiltration under high pressure and shear forces.

• 5 Misconceptions About PFAS Removal Technologies

  This article will explore five common misconceptions about GAC and IX technologies for PFAS removal, helping utilities choose effective, site-specific treatment strategies for contaminated drinking water.

• Scope 3 Emissions: A Shared Challenge, A Collective Responsibility

  Despite growing sustainability efforts, our industry lags in climate goals, especially Scope 3 emissions. Discover why bold action and deep collaboration across the value chain are essential for real progress.

• In The Age Of PFAS, Water Treatment Designers Can't Afford To Guess

  Relying on assumptions when designing water treatment systems creates unnecessary financial and operational risks. Adopting predictive modeling and data-driven testing provides the precise, actionable insights required to optimize performance, manage costs, and ensure compliance.

• Viral Disinfectant Efficacy Studies: Key Guiding Factors And Design Elements

  Achieving compliance and safety through Disinfectant Efficacy Studies (DES) is about adhering to regulations and committing to high standards of safety and quality of manufacturing operations.

• Greater Versatility: Multi-Well Inserts Allow For A Two-Chamber System

  Multi-well inserts allowing for a two-chamber system that can expose cell cultures from above and below provide greater versatility and expand research options compared to standard cell culture plates.

• Q&A: Navigating PFAS In Medical Devices

  Explore how PFAS in medical devices pose environmental and health concerns, prompting regulatory scrutiny.

• Track Microbial Contamination In Environmental Water

  Microbial testing of environmental water demands efficient, contamination‑resistant workflows. Discover a membrane filtration technique that offers rapid, reliable colony isolation.

• Ozone Formulas And Conversions

  Learn key ozone formulas, unit conversions, and measurement standards to accurately calculate generator output, concentration, and dosage for effective system design, performance verification, and safe operation.

• Smarter Cell Washing And Pre-Formulation For Allogeneic Therapies

  Discover common pitfalls in cell washing and pre-formulation, including incomplete contaminant removal, manual handling, and throughput issues that compromise product quality and efficiency.

• Elevating Downstream Process Development With Real-Time Data Monitoring

  Learn how real-time monitoring with PAT enhances process control, shortens development timelines, and supports the shift toward continuous manufacturing in biopharmaceutical production.

• From Syringes To Wearables: Formulation's Impact

  High‑concentration biologic formulations for prefilled syringes and on‑body devices enable easier self‑administration, reduce treatment burden, boost adherence, and address complex formulation challenges.

• Recent Updates To The Declaration Of Helsinki Affecting Clinical Trials

  The World Medical Association (WMA) has announced a significant, rare update to its cornerstone ethical document, the Declaration of Helsinki, which guides medical research involving human participants.