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Market Reports
Case study of an integrated continuous biomanufacturing facility cleanroom build
Abu Bhargava from construction expert Skanska discusses how the company converted a 140,000 sqft half-completed space into an integrated continuous biomanufacturing facility that would meet cGMP requirements
Superway: A novel FAB AMC monitoring model using overhead mobile technology
Richard Xu and Nabil Saad from Nikira Labs discuss its FAB AMC monitoring tech that could change the game for the current model of stationary sensors
Germfree CEO Kevin Kyle talks about productising cleanrooms and decentralised manufacturing
The CEO of the 200-person-strong mobile cleanroom and biocontainment expert talks about decentralised manufacturing for CGTs, a new centralised QMS product in the works, and how carefully chosen partnerships can be a game changer
Combustible dust in pharma: An elusive but very real risk
Controlling contamination and controlling hazards simultaneously in today's cleanrooms is difficult, sometimes even oppositional. Many operations have serious gaps that are difficult to reconcile without the proper expertise. J.T. Cochran from CRB Group discusses
What is MTP technology and how does it affect your cleanroom?
What does Module Type Package (MTP) mean for life sciences manufacturing in relation to customised medicines, ease of engineering, and regulatory compliance? Reinfried Kößlbacher from Copa Data discusses
How can containment tech help you meet your carbon emission targets?
Andrew Ellison from containment equipment manufacturer Envair Technology, talks about creating sustainability in both the product itself and in the environment it operates in
Hot button topics in hi-tech facility design and operation
What are some of the key trends and challenges faced by hi-tech companies and how can these challenges be effectively managed? Jo Nelissen from ABN Cleanroom Technology discusses
Water system qualification and requalifications: Considerations for microbial identification
Miriam Guest from Charles River Microbial Solutions discusses considerations for microbial identification, linked directly to the bioburden samples obtained from water systems
Adjusting wet processing equipment for wheelchair users
Rafal Plewko from Felcon discusses how some simple adjustments can be made to wet processing equipment to allow it to be more inclusive and accessible
The complexities of a cleanroom equipment installation
Rafal Plewko from Felcon looks at the equipment technology supplier Felcon’s process of installing process station
Catch up on our free Cleanroom Technology Roundtables
Discover what experts consider to be the hottest topics across the contamination and control industry, from pharmaceuticals to HVAC and beyond
The most common challenges with a cleanroom
Wes Temple, Director of Marketing at AVM Group looks at some of the main issues that can occur day-to-day in a cleanroom or controlled environment
New Dastex CEO Linda Vereycken talks about her next moves
The incoming CEO at garment manufacturing expert Dastex talks about the next steps following the Riverside, Vita Verita and AET acquisitions, as well as what she is noticing in the cleanroom consumables industry of today
Journey of a pharmaceutical cleanroom build: Concept to validation
Xeal Pharma chose Airology to provide a pharmaceutical production cleanroom. Henry Webster from Airology discusses the journey of that build
What is a semiconductor cleanroom sub-fab?
The team at Jimmy Lea P/L discusses the unsung hero of hi-tech production, cleanroom sub-fabs, which require a strict design and construction plan
Case Study: Building a cleanroom for fluid system component production
AVM Group tells Cleanroom Technology about the process of creating a cleanroom for Swagelok Cleveland
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
A look at the DACH cleanroom market in 2024
The DACH region is important within each countries borders, but also beyond them. Cleanroom Technoogy looks at some of the major news headlines coming out of this influential region in the last year
Otect launches N310, a first of its kind cleanroom glove system
Cleanroom Technology talks to PH Group Director, James Sira, about the company's latest product launch, the Otect N310, a cleanroom glove system that offers a solution to the longstanding problem of people contaminating cleanrooms
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
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
What you missed at the 2024 Cleanroom Technology Conference
The 2024 Cleanroom Technology Conference kicked off in Birmingham on the 22nd May. The highly anticipated two-day exhibition and conference saw delegates from NASA, Samsung, and STAXS gather to share knowledge and network
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
Intuitive robotics: a look at telemanipulation software for cleanroom applications
Bill Rusitzky from SRI discusses how intuitive telemanipulation software gives operators fine control over a robotic arm, allowing remote fixes without disrupting cleanroom environments
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Trending Articles
Combustible dust in pharma: An elusive but very real risk
Controlling contamination and controlling hazards simultaneously in today's cleanrooms is difficult, sometimes even oppositional. Many operations have serious gaps that are difficult to reconcile without the proper expertise. J.T. Cochran from CRB Group discusses
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
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
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?
HVAC cleanroom design calculation explained
Mecart's Charles Lipeles dissects the key considerations to factor in the drawing board
Upcoming event
CPhI Worldwide
8–10 October 2023 | Exhibition | Fiera Milano, Italy
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