Market Reports

Otect launches N310, a first of its kind cleanroom glove system

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 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

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

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

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

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

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?

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
Cleanroom cleaning and disinfection: pushing through the barriers to change

Cleanroom cleaning and disinfection: pushing through the barriers to change

Highly regulated industries like pharma can be resistant to change in the face of stringent hurdles for compliance, but how can manufacturers implement continuous manufacturing into their cleaning and disinfection? Matt Cokely from Ecolab discusses
USP < 797 > Viable Air and Surface Sample Reports: 3 common errors

USP < 797 > Viable Air and Surface Sample Reports: 3 common errors

Sterile compounders often make errors in testing and reporting, this can be in misrepresentation of processes, incubation times, and even the reality of 0 as a reporting number. Abby Roth from Pure Microbiology talks through 3 common errors
The building blocks of cleanroom compliance

The building blocks of cleanroom compliance

How to deliver regulatory considerations throughout the entire cleanroom project lifecycle. Written by Joan Benson and Simon Rice from Angstrom Technology in the UK explain
Enzyme Indicators: Enhancing the H2O2 bio-decontamination validation lifecycle

Enzyme Indicators: Enhancing the H2O2 bio-decontamination validation lifecycle

The Protak Scientific team explains how Enzyme Indicators are transforming bio-decontamination processes
Navigating the IPA supply chain: the essential role of IPA in cleanroom hygiene

Navigating the IPA supply chain: the essential role of IPA in cleanroom hygiene

With the sudden surge in demand for sanitisers and disinfectants post-Covid, supply chains experienced unprecedented disruptions. One essential product caught in the crossfire was Isopropyl Alcohol (IPA), which became a critical resource during the viral outbreak. Elizabeth Norwood from MicroCare explains
Cleanroom Technology Conference Singapore 2023: Day two review

Cleanroom Technology Conference Singapore 2023: Day two 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 Technology Conference Singapore 2023: Day one review

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!
Use of new ISO 14644-17 cleanroom standard in contamination control

Use of new ISO 14644-17 cleanroom standard in contamination control

In 2021 the ISO 14644 cleanroom standard part 17 on the control of macroparticles with the title “Particle deposition rate applications” was published. But how does it work in real life application? Koos Agricola from Brookhuis explains

Trending Articles

  1. How to design your pharmaceutical facility disinfection programme: Development, validation, and implementation The development, validation, and implementation of a robust disinfection programme are critical components of Good Manufacturing Practices (GMP). James Polarine, Matt Hofacre and Tony Cundell explain what you need to do
  2. Cleanroom Technology Awards 2026: The winners The winners of the Cleanroom Technology Awards 2026 have now been revealed. The 2026 edition brought together some of the most forward-thinking organisations in the industry, recognising innovation, technical excellence, and impactful advancements across cleanroom design, operation, and technology
  3. API production: Cleaning equipment between batches Cleaning is an essential part of the API production and it’s important to ensure that all traces of the previous batch are removed before the start of the next one, Pat Downs, Cleaning Co-ordinator at Cambrex discusses
  4. Annex 1: How new draft impacts cleaning and disinfection in cleanrooms The v.12 draft update to EU GMP Annex 1 has laid out how cleaning and disinfection should be considered ‘together’ within a documented contamination control strategy
  5. Semiconductor fab design: What do you have to consider for effective plant layout? A well-designed layout optimises workflow, ensuring that materials and personnel move efficiently through the cleanroom. So what needs to be established to achieve this? The team at Jimmy Lea P/L discuss

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