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Market Reports
Think before you wipe
There is no one-size-fits-all for wipes. Understanding facility priorities, material makeup and absorbency is essential to choosing the right one for the task, says Emily Peck of MicroCare
Butterfly valves: Containment and monitoring for API transfer
Michael Avraam of Chargepoint Technology writes about systems that are critical to preventing HPAPIs harming staff and the bottom line
Europe market report: Playing the waiting game
Demand for cleanrooms, products and services is on the rise in Europe despite Brexit uncertainty. Players in the region say biopharma and the new GMP Annex 1 requirements are key drivers of growth
Grant Merrill | AES Clean Technology CEO
Looking back on 25 years in the business, the mechanical engineer spearheading AES tells CT about the strategy moving the company to pole position in the market
Guide to commissioning and qualification
The specific steps companies should follow to complete a cleanroom project, be it a new build or upgrade, are explained in this guide by Mack Powers, Integrao President
GMP Annex 1: A new dawn in cleanroom garment selection
The new set of guidelines will compel manufacturers to change their approach to contamination control including the way they think about cleanroom apparel, as Jean-François Teneul, Life Sciences Market Leader, DuPont, explains
Factoring the uncertainties in cleanroom design
Align your furniture selection to company culture, SOP and continuous improvement if you plan to make your cleanroom fit for purpose, says Sue Springett of Teknomek
A systematic approach to indoor airflow in operating theatres
Research underway in Germany seeks to identify the optimal indoor airflow to employ during surgeries that prevent the risk of infection. Benjamin Zielke, Valeria Hofer, Hansjörg Rotheudt, Anne Hartmann, and Martin Kriegel, explain
Precision cleaning explained
Cleaning to perfection is a sophisticated process and yet vital to product integrity. Dr Brent Ekstrand, VP of Science & Technology at Astro Pak, sheds lights on contaminants and the tests performed to measure them
A strategy for wireless monitoring compliant with 21 CFR Part 11
Paul Daniel, a Vaisala regulatory expert, gives tips for best housekeeping of electronics signatures and records
Real-time feedback for smart energy usage
The Intelligent Cleanroom Control System, a brainchild of EECO<sub>2</sub>, delivers real-time optimisation, demand-based control and fail-safe retrofitting. Keith Beattie, Life Science Lead, explains
Air filtration: Advantages of PTFE materials
Air filter media built with PTFE, the synthetic fluoropolymer of tetrafluoroethylene, has many advantages when it comes to air filtration in cleanrooms and PPE. Robrecht Hendrikx, Market Manager for venting and filtration at Japanese manufacturer Nitto, explains
Choosing doors for food processing facilities
Sheree Headspith of Dortek walks through the qualities and requirements for selecting the right set of doors for food processing areas
Biocide and mop: Powerful combination
The two-in-one system brought to the market by Redditch Medical and HydroFlex keeps biocide and mop separated until application point. A game-changer that only users will appreciate, as Phil Brennan explains
Particle-free production for low fault rates
The growing requirements for circuit-board electronics push manufacturers to integrate clean production into existing processes. Geiger, the German injection moulding expert, demonstrates how enclosures provide a cleaner environment for making plastic components
Building blocks for milk powder manufacturing
Aluminium honeycomb core panels are lightweight and yet boast exceptional strength, a characteristic that combined with non-shedding and incombustible properties make them the material of choice for food processing manufacturers. Elliot Reilly of Puracore, explains
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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
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