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Market Reports
An A-Z of biobased circular plastics
Stefaan Vanhalle from STAXS explains the different types and their characteristics, along with considerations for special packaging requirements in cleanrooms
London Tech Week 2026: Drug discovery acceleration and speedy CFD analysis
Technology leaders from across the world gathered for a week in London to make connections and educate attendees on recent developments
Standardising pharmaceutical sustainability: Speaking to the creators of BSI PAS 2090?
Courtney Soulsby, Sector Development Director at BSI, and Daniel Witte, Director of Corporate Sustainability at the standard’s co-sponsor and project management office, SLR Consulting, discuss their work standardising sustainability reporting and reduce “greenwashing”
What is RMM?
RMM, or Rapid Microbial Methods, is a concept that is the future of cleanroom monitoring, but what is it and what technologies are out there?
What is happening with the cleanroom market in the United States?
Sophie Bullimore looks at some of the major trends and changes taking place in the US cleanroom market in the last year
Choosing a location to build a data centre or fab
Katie Coulson from Skanska Advanced Technology discusses the process by which data centre and fab locations are chosen
Are centralised and de-centralised approaches to CGT manufacturing really that different?
Andrew Scheffler from ScaleReady discusses whether CGT manufacturing should be centralised in large, industrial facilities, or decentralised closer to the patient in hospital-based or regional sites
Skanska's VP Kate Coulson on the company's technology division launch
The VP leading Skanska’s newly launched advanced technology division talks to Sophie Bullimore about the launch and the market landscape that has defined it
Cleanroom Technology Conference 2026: A review of the highlights
Attendees from Lonza, the NHS, ITH Pharma, Guardtech, AstraZeneca, Kingspan and more, have attended a two day event in Birmingham for the cleanroom and contamination control sector
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, automation, glove handling, cleaning processes, and decontamination methods? Dr. Timo Krebsbach and Dipl.-Ing. Frank Lehmann from SKAN answer this and more
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 and Tony Cundell explain what you need to do
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
Pharma sector uses AI agents to reduce IT incident response times, says KTSL
Aaron Perrott, CTO at KTSL, explains how pharmaceutical companies are using AI agents to improve IT response times, reduce MTTR and support faster clinical and operational workflows
Cleanroom compatibility of wafers: Practical guidance on selecting the right analysis methods
Technical Account Manager Kalle Niiranen from Measurlabs reviews key techniques for confirming that wafer surfaces do not carry contaminants that could compromise cleanroom integrity
Advanced therapy production: A real-world business case for an open RABS upgrade in aseptic production
Thierry Bettinger, R&D Director from Bracco, explains the company’s rationale behind upgrading its Geneva pilot plant with an open Restricted Access Barrier System (RABS) ahead of BubbleGen product line launch
“Operationally net-zero cleanroom laundry”: The details on the £20m project as of now
Sophie Bullimore talks to Micronclean Directors, Greg Cochran and Sophie Harris, about the company’s recent £20m project
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Trending Articles
Cleanroom Technology Awards 2026: The winners
The winners of the Cleanroom Technology Awards 2026 have now been revealed. The 2026 edition brought together some of the most forward-thinking organisations in the industry, recognising innovation, technical excellence, and impactful advancements across cleanroom design, operation, and technology
Standardising pharmaceutical sustainability: Speaking to the creators of BSI PAS 2090?
Courtney Soulsby, Sector Development Director at BSI, and Daniel Witte, Director of Corporate Sustainability at the standard’s co-sponsor and project management office, SLR Consulting, discuss their work standardising sustainability reporting and reduce “greenwashing”
Tips for particle concentration compliance under ISO 14644-1:2015
Apply these six steps to make your cleanroom fit for the new standard, says Hasim Solmaz, Lighthouse Worldwide Solutions
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What is happening with the cleanroom market in the United States?
Sophie Bullimore looks at some of the major trends and changes taking place in the US cleanroom market in the last year
Cleanrooms: solving the mystery of recurring low level contamination
Dr Laurie Smith reviews her research that identified bacteria on cleanroom garments to solve the mystery of recurring low-level contamination in a facility
Upcoming event
CPhI South East Asia
08-10 July 2026 | Exhibition and Conference | Bangkok, Thailand
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