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Market Reports
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
Interview with David Lindholm | KeyPlants
The Head of Sales with a history of chemical engineering and working at pharmaceutical CDMOs, discusses the demand for shortened lead times, the benefits of the company’s recent acquisition, and putting yourself in the client’s shoes
Cleanroom target setting for a sustainable facility
COP26 has reinforced how catastrophic world climate change has to be addressed by all sectors. With reports at the conference stating that life sciences contribute more CO<sub>2</sub> emissions than even the semiconductor industry, this especially applies to cleanrooms and their management. Jamie Young from EECO<sub>2</sub> explains
Vision 2022: new year, new cleanroom
What are likely to be the top headlines of 2022? From new design concepts, to global shortages, to fresh businesses popping up worldwide. If 2020 was a global emergency and 2021 was the recovery, 2022 is looking to be the renaissance
India cleanroom market report | Nothing but potential
The current focus on quality improvements and localised production in India are happening alongside the huge boom in demand. Cleanroom consumables and equipment providers in the region talk about their experiences with this and their interest in how the post-pandemic era will play out
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Trending Articles
The importance of growth promotion testing
Given the critical nature of microbiological quality tests which are employed to ensure that pharmaceutical products are safe for human use, it is in turn essential to undertake quality control (QC) tests to ensure that the culture media being used for these is fit for purpose and performs properly. Cherwell Laboratories' Steven Brimble explains
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
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!
Cleanroom tightness and room pressurisation: Discrepancy?
A cascaded room-pressure regime has been considered for decades to prevent cross-contamination of different processes. But Harald Flechl from ISPE says today's tight cleanrooms must have leaks to ensure a room-pressure regulation - so why should we build tight cleanrooms?
How-to guide: Pass box qualification
Material transfer equipment plays an important role in minimising contamination risks during the manufacturing process. Industry expert, Jesus Casas, gives an overview of available pass boxes and a step-by-step explanation on how to qualify them appropriately
Upcoming event
Cleanroom Technology Conference UK
22–23 May 2024 | Conference and Exhibition | Birmingham, UK
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