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Market Reports
Adaptable and fast builds from 2017
Many countries saw increased investment in new cleanrooms in 2017 but it was very sector specific. Meanwhile the application of new design and construction techniques has made the process faster, with fewer snags. Susan Birks summarises the year’s trends in cleanroom construction
Eco-friendly disposables wanted
Last year was a challenging year for the cleanroom apparel market, which was hit with changes in the PPE directive along with a call for more environmentally-friendly solutions. Charlotte Alldis rounds up 2017 most significant product launches providing a solution to these complex issues
Performance validation: HPAPI containment testing in a risk-based era
Taking a more automated approach to validation testing paves the way to capturing more repeatable and reliable data, thereby improving levels of containment performance
Telstar unveils 'smart' cleanroom HVAC system
Telstar has designed an innovative HVAC control system that provides automatic regulation in cleanrooms and saves over 40% in energy consumption
Jenoptik expands manufacturing capacity with new Class 5 cleanroom
Jenoptik has tripled cleanroom space at its Jupiter, Florida location to address increased global demand for optical systems
Protecting downflow booth performance for safe operation
Downflow booths provide a safe environment for workers handling potentially hazardous powdered raw materials but to ensure continuous safe operation, regular inspection and maintenance programmes should be in place. Hosokawa Micron highlights the main considerations
The acid test: pH measurement of water quality
For decades pH measurement has been the mainstay of water quality testing in cleanrooms and labs. However Mark Bosley, Business Support Divisional Manager, SUEZ Water Purification Systems, outlines some common pitfalls
Cleaning cleanrooms
Cleanroom cleaning requires many specialised products. Dr Tim Sandle, head of microbiology, Bio Products Laboratory, addresses the importance of product selection and cleaning techniques in the pharmaceutical manufacturing environment
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Trending Articles
Walking the tightrope: a look at air change rates
How can companies design their cleanrooms in order to reach the air change rates required by ISO? Words by Simplex's Jerry Cross
Cleanrooms: What is the difference between clean-up period and recovery time?
The implementation of the new Annex 1, and references to the ISO 14644 family of cleanroom standards have raised questions around the "Recovery time" and the "Clean-up period." Nataša Štirn from Klimer and ICCCS Chair Conor Murray discuss
GMP Annex 1: Validation of disinfectants on cleanroom surfaces
Published in August 2022, for implementation in August 2023, Karen Rossington from Contec looks at the revised version of EU GMP Annex 1 expanded and clarified the regulatory requirements of cleaning and disinfection in life science cleanrooms
Virucidal testing of cleanroom disinfectants
In “normal” times, with the exception of live vaccine manufacturers, control of viruses in cleanrooms is not usually the highest priority within contamination control. Viruses need a host to survive, as they are obligate parasites, just nucleic acid surrounded by a protein that can only replicate within a host cell, so their ability to survive on hard, dry surfaces is minimal. Contec’s Neil Simpson explains
Incubating settle plates: Understanding growth patterns and when things are going wrong
Steven Brimble from Cherwell Laboratories discusses why it is important to your environmental monitoring regime to understand growth characteristics of common cleanroom contaminants and how morphology shifts over time on various media
Upcoming event
CPhI South East Asia
08-10 July 2026 | Exhibition and Conference | Bangkok, Thailand
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