Cleanroom Editorial and News

31. Why Is 50% The Limit For Particle Counting Efficiency Sizing Thresholds In Cleanrooms? 6/18/2024

    Particle counting efficiency is vital, especially when using optical particle counters. Learn why 50% is the limit for counting efficiency sizing thresholds in optical particle counters.

32. Does My Cleanroom Facility Need A Residue Removal Step? 3/28/2024

    Explore the challenges presented by the residues left behind by disinfectant solutions in cleanrooms as well as effective strategies for their management.

33. Advanced Isolator Tech Boosts Manufacturing Efficiency And Quality 7/30/2024

    Isolator technology can run continuously over several days, minimizing operator interaction and other opportunities to introduce contamination — ideal for high-volume, time-limited production runs.

34. Particle Measuring Systems And Pharma Integration Introduce The BioCapt® Single-Use AutoM Microbial Impactor For Automated Microbial Air Sampling 6/10/2024

    Particle Measuring Systems (PMS), a global leader in contamination monitoring, and Pharma Integration, a company that specializes in innovative robotic solutions for small volume fill-finishing for next generation injectable drugs are proud to announce the launch of the BioCapt Single-Use AutoM Microbial Impactor.

35. Compressed Gas Contamination: Guidelines For Control In Aseptic Manufacturing 10/18/2024

    Explore key guidelines for preserving the purity and quality of compressed gas, with an emphasis on contaminants, monitoring, and preventive maintenance practices.

36. A Brief History Of Aseptic Processing 3/27/2025

    From Bunsen burners to advanced isolators, aseptic processing has evolved significantly. Delve into the evolution of this crucial manufacturing method, from its early sterilization techniques to today's highly controlled and regulated environments.

37. Formulation Development Experience For Effective Particle Identification 1/14/2026

    Combining advanced analytics with deep formulation knowledge enables precise root-cause analysis, preventing manufacturing delays and ensuring that products remain high-quality and safe for patients.

38. Data Management Considerations For Environmental Monitoring 6/18/2024

    Learn what data management factors to take into consideration when setting up an environmental monitoring system in a pharmaceutical manufacturing facility.

39. Key Topics And Trends In Aseptic Filling 1/9/2026

    Aseptic filling is vital yet often guided by outdated practices. Discover expert insights on modern technologies, evolving regulations, and data-driven strategies to improve compliance and reduce risk in this critical manufacturing step.

40. Optimizing Cleanroom Cleaning And Disinfection To Meet Annex 1 Requirements 12/27/2024

    Explore Annex 1 updates on contamination control in pharmaceutical cleanrooms, emphasizing cleaning consistency, training, advanced tools, and technologies to achieve regulatory compliance.