Market Reports

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

Cable ties for cleanrooms: Antimicrobial and metal-detectable

The Panduit team discuss why even cable ties and mounts need to have specific properties for use in hygiene-sensitive areas

Cleanrooms: What is the difference between clean-up period and recovery time?

The implementation of the new Annex 1, and references to the ISO 14644 family of cleanroom standards have raised questions around the "Recovery time" and the "Clean-up period." Nataša Štirn from Klimer and ICCCS Chair Conor Murray discuss

Trending Articles

  1. Pharmaceutical waste: What do I do with it? Emma Cooke from Envirovue discusses the many hazardous elements of pharmaceutical waste and the importance of effective management and compliance
  2. Pharma sector uses AI agents to reduce IT incident response times, says KTSL Aaron Perrott, CTO at KTSL, explains how pharmaceutical companies are using AI agents to improve IT response times, reduce MTTR and support faster clinical and operational workflows
  3. 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
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    Annex 1 and “first air”: What is it and how is it used? First Air as a concept is a major update in the new Annex 1 to continue global harmonisation of regulatory standards, but what is it and how is it used in the new document to improve clarity and compliance? Josh Russell, VP of Sales and Marketing at AST discusses
  5. 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

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