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  1. When are isolators or RABS essential rather than optional? The new EU GMP Annex 1 clearly stipulates that the absence of a barrier system must be thoroughly justified, but when is this, and what does it mean for isolator configuration,...
  2. How to design your pharmaceutical facility disinfection programme: Development, validation, and implementation The development, validation, and implementation of a robust disinfection programme are critical components of Good Manufacturing Practices (GMP). James Polarine, Matt Hofacre...
  3. Pharmaceutical waste: What do I do with it? Emma Cooke from Envirovue discusses the many hazardous elements of pharmaceutical waste and the importance of effective management and compliance
  4. Cleanroom Technology Conference UK 20-21 May 2026 | Conference and Exhibition | Birmingham, UK
  5. Camfil acquires Bion to strengthen molecular contamination control offering The clean air specialist has acquired Spanish filtration and adsorbent manufacturer Bioconservación (Bion) to expand its molecular contamination control capabilities

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Design & Build

G-CON Manufacturing announces acquisition of Atmos-Tech Industries

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GCS scales up cleanroom panel production with automated line

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Design & Build

Top 10 cleanroom problems that can be prevented via preventative maintenance

Berk Mollaoglu from G-CON discusses how to avoid the problems that can result from the the general wear and tear of time in a cleanroom
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Enhancing cleanroom design: a deep dive into walk-on ceilings

GCS, a leader in cleanroom panels, explores the challenges, design considerations, and essential features of world-class walk-on ceilings for cleanrooms
Design & Build

G-CON to showcase hybrid cleanroom solutions at INTERPHEX

Company highlights Optimized by Design for scalable, adaptable controlled environments
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