Cleanroom Whitepapers and Case Studies

  1. Could RFID-Based Unit-Level Traceability Be Key To Operational Excellence? 9/5/2023

    Radiofrequency identification (RFID)-based unit-level tracking solutions for prefilled syringes are poised to help pharma manufacturers address key risks and costly bottlenecks related to the fill-finish process.

  2. Emergency Containment Solutions And Disaster Support For A Liquid Storage Facility 5/12/2023

    Discover how a successful partnership between an environmental company and a liquid storage facility helped mitigate a disaster from escalating and gave them the rapid response they needed. 

  3. Mobile USP 797 and 800 Sterile Compounding Pharmacy Cleanroom Trailer 6/26/2024

    Learn about the USP 797 and 800 compliant drug compounding pharmacy cleanroom trailer that was supplied to Duke Raleigh Hospital during renovations of its main building to support the heavy workload.

  4. Single-Use Innovation For The Future Of Therapeutic Manufacturing 1/28/2025

    Gain insight into these end-to-end plasmid DNA solutions, leveraging robust cGMP-compliant processes and single-use manufacturing platforms to accelerate your cell and gene therapy programs.

  5. Development Of Endothelial-Cord Cell Banks And Blood Stem Cell Products 5/28/2025

    Leverage our proven cGMP expertise in cell therapy manufacturing, from primary tissue processing to large-scale production for clinical trials.

  6. Calcium Carbonate Vs Titanium Dioxide: Why Particle Engineering Matter 11/10/2025

    Discover how particle-engineered calcium carbonate offers a viable alternative to titanium dioxide in tablet coatings, achieving good opacity, process efficiency, and comparable tablet properties.

  7. How To Avoid Sticking And Picking In The Tableting Industry 9/23/2024

    Review strategies to mitigate sticking and picking risks in the tablet industry, and learn how you can foster improved tablet production processes, ensuring higher quality and consistency.

  8. Advances In Regulations For Viable Environmental Monitoring 2/21/2025

    Viable air monitoring is critical for environmental monitoring programs in pharmaceutical manufacturing. Explore current regulatory standards as well as the impact of the EU GMP Annex 1 revisions.

  9. Key Considerations For Selecting A Solenoid Valve In Health & Science Applications 10/7/2025

    Solenoid valves are vital in medical devices, enabling precise fluid and gas control. Explore customizable, high-reliability valves that optimize performance while conserving space, weight, and power.

  10. Boosting CMC Regulatory Efficiency In Gene Therapy 9/30/2024

    Ensure your business stays ahead in today’s complex regulatory environment by implementing robust regulatory affairs strategies that streamline compliance and product approvals.