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Market Reports
Automating HEPA filter scans in barrier systems
Syntegon and InfraSolution discuss how the two companies have launched the first system for automated HEPA filter scans in barrier systems. Thomas Kosian and Christian Dorfner explain
Digital environmental monitoring: catch failures before they happen
There are many benefits to a day-to-day digital monitoring process, but how does it deal with a contamination event in the environment. This is where the benefits go from operational efficiency to operational agility explains Toon Lambrechts from MyCellHub
A guide to choosing the best particle sample point location
Particle counting in pharmaceutical applications can be clearly segregated into one of three categories: certification, qualification and monitoring. Each category requires a different approach as explained by PMS' Mark Hallworth
What is happening in the cleanroom market in 2022's DACH region
A look at the trends and major business deals through Germany, Austria, and Switzerland in a time of great turmoil across Europe
Interview with PathogenDx founder Milan Patel
The microarray testing company CEO discusses setting up a company and product to penetrate the microbiology testing market. The entrepreneur also dives into the importance of pathogen testing in the cannabis market
Opportunity mapping: Deploying risk analysis to improve transfer disinfection
A look at improving transfer disinfection and residue management, focusing on a UK case study following the use of the software at a pharmaceutical manufacturer and a demonstration of how areas for improvement can be identified and resolved
A systems approach to the future of cleanroom manufacturing flexibility
To help assure patient access to sterile injectable (SI) medications and meet the current needs of developers, aseptic facilities must be fit for a future of flexibility. What’s the secret to creating cost-efficient aseptic capacity and a facility that is truly flexible? Grant Merrill from AES Clean Technology discusses
Interview with HVAC filtration expert Andrew Marshall
UK-based filtration expert Triple Air Technology's Sales and Marketing Manager discusses his unconventional route into the cleanroom sector, how the pandemic changed the industry, and how environmental policies are impacting new builds
Regulatory warning letters in pharma: What can we learn post-COVID?
A look at how the COVID-19 pandemic impacted FDA inspections and the trends that have now cropped up reflecting industry changes. Mirna Vazquez and Jessica Rayser from Charles River Laboratories reflect on these trends
Book your exhibitor space at Cleanroom Technology Conference Singapore!
Join leading exhibitors from the industry including Ecolab, Fisher Scientific, Micronclean, Tofflon, UV Medico, Guardtech Group, STERIS at this year's event
Cleanroom contracting: Should you look across the border?
There are many advantages to hiring a local contractor, but limiting your search to your country's borders may be limiting your potential. CRB's Rasmus Kidmose looks at the factors on either side of the discussion
A look at the US cleanroom market | Beyond the engineering
The infection control sector is intrinsically intertwined with the engineering sector, and any major change in demand and needs causes a domino effect in the other. The US market is a prime example and speaking to the experts reveals why
Containing potent product manufacture in a multi-product facility
With the source of HPAPI manufacturing in huge flux between big pharma players, specialised start-ups, and the trusty CDMO, companies need to appreciate the importance of a proper New Product Introduction strategy Metrics Contract Services' Anshul Gupte explains
Interview with BIM Manager Joe Murphy from Connect 2 Cleanrooms
As Building Information Modelling has become a more common practice, your BIM Manager has become more and more important. Joe Murphy talks about his career journey and some important lessons he has learnt in modelling a cleanroom project
Avoiding delays in your next cleanroom facility project
All the Gantt charts in the world can not make a cleanroom project run smoothly if things have been missed off them. Here are some tips from industry veterans to avoid setbacks from Mecart's Charles Lipeles
Isolators on a film set: An oddjob for Envair
Working as a film set consultant is not your average day for those in the controlled environment sector, but who better to bring a top-secret research lab to the big screen than the experts themselves. Envair's Susie Lee-Kilgariff talks about the experience
Common problems with the plate count method in cleanroom compliance
Traditional manual methods for microbial enumeration in monitoring cleanroom cleanliness have stayed relatively constant over the years, but what is changing this? Mark Newton and David Jones from Rapid Micro Biosystems explain
The regulations don't go far enough: Glove permeation testing in chemotherapeutics
Ansell Senior Director of Project Management, Eric Boeckmans, talks to <i>Cleanroom Technology</i> about why testing glove permeation ‘in-use’ is key to safe handling
Interview with lean construction expert Tammy McConaughy
The CRB Director of Lean Delivery discusses her training in the lean concept, her introduction to the cleanroom sector, and how the two are a perfect match
Understanding the demands of small batch sterile fill
Manufacturing drugs via small batch sterile fill-finish comes with unique considerations, but what are these, and what is the sector looking like after two years in a pandemic? Alex Garner, Khanh Ngo Courtney, and Frank Manella from Element explain
20 questions with Lonza HPAPI containment expert
An in-depth discussion about Highly Potent APIs (HPAPIs) and their containment with Christian Dowdeswell VP, Head of Commercial Development, Small Molecules at Lonza
A guide to common sterile processing contaminants
Why are some organisms more common cleanroom and sterile processing contaminants? To understand this, we must look to Darwin as Chris Bartlett from Lexagene explains
Harmonisation of Annex 1 and ISO 14644-1: A deeper look
Alexander Fedotov from Invar explains that the harmonisation of standards seems to be a driving force for setting particle limits and why this may not always result in logical scientific decision making
How to analyse limit breaches
Environmental monitoring limit breaches are one of the first things quality control professionals look at when reviewing their data. But how do you set these levels to determine the state of microbiological control within the cleanroom? Microgenetics' Edward Webber explains
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A look at solar manufacturing cleanrooms in the US
Blake Hodess walks through the needs of the solar manufacturing facilities within the US industry
The details of dust extraction in controlled environments
To choose the right machine, the nature of the dust and the statutory regulations for its handling and removal, as well as classification of the machine and filter technology, must be considered. Daniel Took from archer reminds us, the lower the Threshold Limit Value (TLV) for dust, the higher the health risk
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
Today's highlights: Day 1 at the Cleanroom Technology Conference 2025
Talks have begun and exhibitor stands are open at this year's event. Almost 400 people are gathered in Birmingham, with attendees from Micronclean, Guardtech, AstraZeneca, Kingspan and more
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
Upcoming event
ISPE Singapore
28-30 August 2024 | Conference and exhibition | Singapore
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