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Market Reports
A to Z of an effective monitoring programme
A successful monitoring process allows control of contamination for regulatory or product yield reasons. John Merrill from C2C explains monitoring results can be used for trend analysis by comparing data with subsequent air samples, and alert and action levels can be set for results outside of set acceptable thresholds
Clothing solution for EU GMP Annex I
Only single-use cleanroom apparel will help sterile product manufacturers improve compliance with the new guidelines, as Franck Bureth of Kimberly-Clark Professional explains
Jo Nelissen | ABN Clean Technology
In an interview, the founder and CEO of Belgium-based cleanroom engineering company discusses the issues of 2020 and his opinion on the growing cleanroom practices and technologies of today
Speaking opportunities for Cleanroom experts
Industry experts from the cleanroom industry are invited to submit their presentations for the Cleanroom Technology Conference in July
Germany market report | Supporting the vaccine race
A country that is taking on many fronts of the pandemic response, Germany has a well-known pharmaceutical landscape and an enviable cleanroom backbone. But is it enough?
Should technology based ARMMs be more widely adopted?
New technologies now exist that can reduce the time taken to detect viable particles by almost comical percentages, while also detecting and distinguishing inert ones. Therefore, it is puzzling why the uptake of ARMM devices in aseptic pharma manufacturing seems so slow
Validating VPHP bio-decontamination of FFP masks
DeconBox is a Vapour-Phase-Hydrogen-Peroxide bio-decontamination system that allows FFP2 and FFP3 masks to be reused. Riccardo Volta and Giacomo Nicolini from Comecer explain the process of validating the mobile, purpose-built system for use in controlled settings
Manipulators: A gamechanger in radiopharmaceutical production
For many years manipulator technology has stagnated, but recently, remotely controlled manipulator design has shown a leap forward. Jim Peterson from Central Research Labs discusses the variety of these machineries that help keep operators and radioactive material separate
Martin Birch and Peter Makowenskyj| G-CON Manufacturing
The modular construction movement is an unstoppable train at this point. In an exclusive interview, two G-CON Directors discuss the trajectory of this expanding technology, and how multiple global crises are changing business on both sides of the pond
AMC monitoring in fabs with spectroscopic methods
Airborne molecular contaminants clearly affect semiconductor yield and can’t be completely removed by modern filters in cleanroom fabs. Thomas Benoy from the $2.1m MetAMCII project says it is aiming to address the increasing need for measurement capabilities from the low ppb to the ppt in real time with low uncertainties
Cleanroom Conference and Manufacturing Chemist Live 2020 to go virtual
The virtual event taking place on 10-11 November 2020 will provide delegates with full access to the Manufacturing Chemist Live, Cleanroom UK, India and Singapore content and exhibitors
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?
Milos Perovic | Termovent
In an interview with Cleanroom Technology, HVAC specialist COO and Head of the Cleanroom division was proud to discuss the behind-the-scenes importance of controlled environments during a time of pandemic
The evolving role of a contamination control strategy in Annex 1
A Contamination Control Strategy is a cyclical process designed to prompt the manufacturers to identify and resolve risk. With the 2020 draft update to Annex 1, David Keen from Ecolab looks at the interesting specific impacts of the changes on the role of a well-designed CCS
Adoption of rapid methods for QC microbiology in biopharmaceuticals
Rapid turnaround times and high sensitivity are essential for microbial QC testing. David Jones from Rapid Micro Biosystems explains that by the time a traditional test is completed, it can be difficult to rewind several days into the past and pinpoint the cause of a contamination event
The benefits of decentralised air handling
Performance requirements and sustainability targets can sometimes be at odds in the cleanroom world, but decentralised air handling system design can actually benefit both says Connect 2 Cleanrooms' Sam Armer
Cleanroom Conference and Manufacturing Chemist Live events set to go ahead
The co-located events will go ahead in October with new safety measures in place, after being postponed from their original date at the start of summer due to COVID-19
Nano-copper technology for antimicrobial surface design
Research has shown that copper ions are released when microbes land on a surface and can kill them, but regular copper can cause an uneven surface that is ideal for the microorganisms to adhere to. Selina Ambrose from Promethean Particles discusses nano-copper as a novel technology aiming to address this with liquid dispersion
Isolators: The beginnings of a new trend in Asia
To date, very few filling and closing machines have been installed in Asia. Aprogen Biologics and Optima Korea are both convinced that this will soon change as they install an isolator system in South Korea
Reginald Fernandes & Jamie Tempest | Reading Scientific Services
When taking its first venture into cleanroom technologies and sterility testing, RSSL picked a balanced team of microbiologists with different specialisms to guide them
UK market report: Cleanroom business from Brexit to COVID-19
Uncertainty is a word all UK operators are well-acquainted with by now, from Brexit to a global pandemic. Speaking to directors of companies in the thick of it shows how resilience and preparedness is helping them transition to the ‘new normal’
Isolator transfer design for ATMP products
A challenge posed by the increase of closed systems is the transfer of semi-finished products without losing the aseptic conditions required by regulations. A new study has tested a transfer system aiming to offer biocontainment without losing cell viability of ATMP products
Putting disinfectant to the test: Designing a field trial
Cleaning and disinfection is a process that can become very elaborate in cleanrooms. Tim Sandle in conjunction with Ecolab Life Sciences discusses designing a thorough and reliable field trial to test this process
Annex 1: How v.12 update impacts cleanroom cleaning and disinfection
The latest draft of sterile manufacturing guidelines may change again, but Matt Cokely from Ecolab says the direction of travel for the guidance is reasonably clear with regards to the guidance for cleaning and disinfection as an integral part of a Contamination Control Strategy
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Trending Articles
AVM Group: The history behind the cleanroom industry merger
US-based cleanroom and containment expert AVM Group talked exclusively to Cleanroom Technology about the history behind the separate companies and the project collaborations that led to the landmark merger
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
AST Chief Technical Officer talks designing new isolator tech to address the pharma industry's pain points
Cleanroom containment expert AST’s CTO and VP of Customer Service, Steven Ng, talks to Cleanroom Technology about the creation of the company’s new isolator technology and how the industry trends and pain points were taken into account
Continuous cleanroom monitoring: A look at automated settle plate handling
Continuous monitoring is becoming increasingly important in the most critical areas like class A and B of aseptic manufacturing or ATMP production, Miriam Schönenberger and Florian Blum from MVB discuss how it can be implemented in the best possible way
How CFD simulation is applied in semiconductor cleanrooms
The Jimmy Lea team discuss how Computational Fluid Dynamics (CFD) can help predict airflow, temperature patterns, pressure differentials, as well as model for fire events predicting smoke and CO<sub>2</sub> exposure
Upcoming event
ISPE Singapore
28-30 August 2024 | Conference and exhibition | Singapore
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