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Market Reports
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
Contamination in a changing food production industry
The European food sector has changed significantly over the last three years. The influence equipment manufacturers have had on cross-contamination and standard cleaning requirements is key to enabling these advances
Cleaners and carrier fluids: Preventing contamination in medical device production
Modern cleaning and coating fluid technologies and associated vapour degreasing equipment provide consistent and reliable device cleaning. However, these modern cleaning fluids offer added benefits beyond this
COVID-19: Testing for surface and air presence
Protecting healthcare workers against coronavirus requires a multi-faceted approach. Rapid testing technology for aerosolised and surface virus are two ways that ensure detection for an effective management strategy
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
Halden Shane | TOMI Environmental Solutions
Leading a decontamination company during an infectious disease outbreak is no mean feat. Founder and CEO of TOMI, Dr Halden Shane, explains why its Ionized Hydrogen peroxide is a great weapon in your arsenal
Guide to implementing a VHP system for facility biodecontamination
Vaporised hydrogen peroxide biodecontamination systems can be installed and integrated into a plethora of cleanrooms or suits. Here John Klostermyer, VHP Application Project Manager at STERIS, provides some tips for drafting a process-oriented User Requirement Specification
Social distancing in a lab
While rigorous hygienic standards are already in place, new practices are required to help those in the cramped confines of cleanrooms and labs during the COVID-19 pandemic. Sue Springett, Commercial Manager at Teknomek, discusses what needs to be evaluated; such as the problems in crowded gowning rooms and the conflicts of priorities with air flow
Gaby and Ute Schilling | Schilling Engineering
German cleanroom company Schilling Engineering was founded more than 20 years ago. Now the founder and CEO is preparing his twin daughters to become his successors
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
Matts Ramstorp | BioTekPro
The CEO of the Swedish training and consultancy company looks back on 30 years in the business and argues the “know-why” is the real knowledge gap in the market
US market report: Biologics and sustainability lead the way
The sentiment is positive among cleanroom solution providers because influx of projects comes from all market segments, and there is further growth in emerging applications
Sitting down with TRU Cleanroom Cleaning co-founder Vanessa Morini
The Co-Founder of the cleanroom cleaning company in Genk builds on her process technology and validation expertise to explain why TRU is filling a gap in the market
Aseptic manufacturing: The robots are coming
Two collaborative projects between industry and two Irish universities are paving the way for autonomous robots in the pharma industry. Writes PM Group's Dave Wolton
Hi-tech cleanroom: Humidity control to the forefront
John Barker, Managing Director of Humidity Solutions, on the requirements to achieve high yield in the manufacture of lithium-ion batteries
Optimise desiccants with 3D validation software
Baltimore's CFD model brings predictive science to validation. Desiccants are tested for performance over time, bringing cost-efficiency to the forefront. Dr Mark Valentine explains
Amy Meysner | Glass Technology Services
The Chemistry Manager of the UK-based glass specialist discusses delamination risks and says only proactive companies can win the quality control challenge
DNA-driven pathogen detection for cannabis-hemp products
Shortcomings in traditional culture testing leave the industry in search of methods that can enumerate or count the presence of microbes whether dead or alive. Dr Jack Regan presents an alternative
Vision 2020: Cleanroom experts reveal expectations for the year ahead
Some of the leading figures in the contamination control industry comment on what lies ahead
Man or machine: The workforce of cleanroom 5.0
If full automation were technically possible, would it be legally achievable, ethically justifiable or economically sensible? The race between men and machine is on. Dr Gernod Dittel explains
Challenging disinfectant residues as per GMP Annex 1
Karen Rossington of Contec analyses commonly used cleanroom disinfectants to shed light on the best approach to tackle residues that are left on surfaces
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Trending Articles
Today's highlights: Day 1 at the Cleanroom Technology Conference 2025
Talks have begun and exhibitor stands are open at this year's event. Almost 400 people are gathered in Birmingham, with attendees from Micronclean, Guardtech, AstraZeneca, Kingspan and more
Identification methods for bacterial isolates
Identification of bacterial isolates provides vital information for companies undertaking environmental monitoring programmes, but methods vary greatly. Vikki Warren from NCIMB discusses
Disinfectant efficacy testing: US vs Europe
There are many standard disinfectant efficacy test methods available in both Europe and the United States but the testing approach is very different and using the tests in the opposing regions is not so easily accepted. Karen Rossington from Contec explains
The cleanroom debate: Epoxy flooring vs raised flooring
There is no “right choice” for the flooring in your cleanroom or controlled environment, but there are aspects to weigh up for a more suited solution. Wes Temple from AVM Group explains
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
Upcoming event
Pharmig Annual Pharmaceutical Microbiology Conference
20-21 November 2025 | Conference | Nottingham, UK
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