Cleanroom Whitepapers and Case Studies

  1. Overcoming HCP Co-Elution Issues Using Cell Line Engineering 5/15/2024

    Product quality assessments revealed that a customer’s therapeutic protein had a range of hydrophobic HCPs. Review a solution that took an alternative approach by utilizing cell line engineering.

  2. Innovation In Filtration 3/18/2025

    Filtration removes contaminants to ensure safety and is essential in various applications, from lab-scale tasks to GMP production. Explore how its simplicity and reliability make it indispensable.

  3. Meeting Local Regulations With Ready-To-Use Buffer Solutions 1/22/2024

    Learn about a ready-to-use, custom buffer solution provided to a biopharmaceutical manufacturing facility in order to help them reduce costs and the amount of time spent on QC testing and validation.

  4. Reducing ADC Timelines With Integrated Development And Manufacturing 4/8/2024

    ADCs have proven to be highly effective in cancer treatment, but their manufacturing poses challenges. Learn how a CDMO partner can help bring these treatments to patients safely and efficiently.

  5. Prefabricated Viral Vector Modular BSL-2LS cGMP Facility In 13 Months 6/26/2024

    Learn about the modular BSL-2LS cGMP facility that was constructed to support 3 processing lines for German-based CDMO Vibalogics as the company sought to expand in the U.S. market for viral vectors.

  6. Improving Efficiency In Contamination Identification 7/11/2025

    Discover how rapid microbial identification using MALDI-TOF improves contamination response, shortens investigation timelines, and enhances efficiency in biopharmaceutical manufacturing.

  7. Comprehensive Compressed Air Assessments: The 5-Step Process 10/10/2024

    The objective of this paper is to define the five steps required in a compressed air assessment. We will use a real-world example with system information from a magnetic materials manufacturer to clearly illustrate each step.

  8. ABSL-3 Facility For Duke (National University of Singapore) 6/6/2024

    Read about a 5-module ABSL-3 facility that was constructed in Singapore, and is used for disease surveillance, research on avian influenza, and other risk group 3 materials.

  9. Enhancing Viral Clearance Prediction And Process Optimization 7/11/2025

    MockV technology enables early, in-house viral clearance assessment, helping biopharma developers improve process robustness, reduce costs, and enhance safety before GMP manufacturing begins.

  10. The State Of Plastics Recycling In BioPharma 8/9/2023

    Recycling plastics from biomanufacturing proves uniquely difficult due to circularity, quality, and infrastructure challenges. Nonetheless, change is underway. Learn how this change is being spearheaded by industry leaders.