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Market Reports
The building blocks of cleanroom compliance
How to deliver regulatory considerations throughout the entire cleanroom project lifecycle. Written by Joan Benson and Simon Rice from Angstrom Technology in the UK explain
Enzyme Indicators: Enhancing the H2O2 bio-decontamination validation lifecycle
The Protak Scientific team explains how Enzyme Indicators are transforming bio-decontamination processes
Navigating the IPA supply chain: the essential role of IPA in cleanroom hygiene
With the sudden surge in demand for sanitisers and disinfectants post-Covid, supply chains experienced unprecedented disruptions. One essential product caught in the crossfire was Isopropyl Alcohol (IPA), which became a critical resource during the viral outbreak. Elizabeth Norwood from MicroCare explains
Cleanroom Technology Conference Singapore 2023: Day two review
Attendees from Asia and beyond attended the Cleanroom Technology Conference Singapore at the start of December. Those that did were in for a treat!
Cleanroom Technology Conference Singapore 2023: Day one review
Attendees from Asia and beyond attended the Cleanroom Technology Conference Singapore at the start of December. Those that did were in for a treat!
Use of new ISO 14644-17 cleanroom standard in contamination control
In 2021 the ISO 14644 cleanroom standard part 17 on the control of macroparticles with the title “Particle deposition rate applications” was published. But how does it work in real life application? Koos Agricola from Brookhuis explains
Your cleanroom equipment: Calculating the carbon footprint
Climate protection is not only dominating public discourse; it is also influencing the way we think about pharmaceutical production processes. Calculating process equipment’s carbon footprint is an important aspect of this. Dr Andreas Mattern from Syntegon Technology explains
What’s wrong with Annex 1
Alexander Fedotov, Director of Clean Technologies (formerly Invar-Project), talks about some of the changes to the new Annex 1 and his reasonings on why there is a lack of sense to them
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
BCT Group's Katia Bougatsou explains the implications of sustainability and geography for the cleanroom market
The Greek cleanroom engineering firm’s MD and HVAC expert talks honestly about her country’s sector, the problems plaguing the push for sustainability in cleanrooms, and how understanding a project scope is key to continued success
XNRGY Climate Systems' Wais Jalali on decarbonising HVAC
A fixture of the HVAC world, the Chairman and CEO of XNRGY, the North America-based sustainable HVAC expert, talks about his career and his take on decarbonising the production process
Case study: The first complete dental clinic in the Netherlands
It took almost all of 2022 to achieve the desired expansion and scale-up of the existing oral clinic in Hoofddorp, The Netherlands, into a complete dental clinic, including OR and X-ray facilities, but the result is impressive!
Does plate choice affect microbial air sampling accuracy?
An investigative study has found that some current microbial air sampling processes may fail to comply with the new EU GMP Annex 1 - it is important to understand how inaccuracies may arise. Words by Cherwell's Hamish Hogg
The safety-first approach that harnesses the power of HPAPIs
Insights into the challenges associated with handling highly potent active pharmaceutical ingredients (HPAPIs) safely. Exploring the use of next-generation containment technology as a means to comply with safety regulations and ensure the safest possible working environment for employees. Jonathan Bardsley from ChargePoint
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
ChargePoint executive Christian Dunne gives his expert take on the sterile and aseptic markets
The Director of Global Corporate Business Development from ChargePoint Technology talks about the sterile and aseptic markets in the past, present, and future and how he is managing the industry going forward
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Development, validation, and implementation: How to design your pharmaceutical facility disinfection programme
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
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
A to Z guide to protective garments
Understanding, assessing, validating and auditing the entire value chain of cleanroom garments is critical to making sure they are fit to play their part in the manufacturing process. Steve Marnach and Matheus Barbosa, DuPont, 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
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
Upcoming event
ISPE Singapore
19-21 August 2026 | Conference and exhibition | Singapore
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