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Market Reports
Guide to wireless dataloggers for thermal validation
New wireless dataloggers deliver accurate thermal mapping with time-saving benefits. Chris Maughan, MD of Thermal Compliance, explains
Passivation: An extra layer of protection for critical equipment
The cleaning process that removes iron from a surface layer of stainless steel alloy can play a pivotal role in biocontamination prevention. Astro Pak experts Daryl Roll and Dr Brent Ekstrand explain
Review: Cannabis Europa 2019
Scientists, businesspeople and politicians backing the regulation of medical and recreational cannabis have taken the stage of Southbank Centre this week to discuss research and business opportunities
Compound semiconductors: Let there be light, speed and power
UK companies get ahead of the curve with investments in R&D and fabrication infrastructure for next-gen electronics. Andy Sellars, Chief Business Development Officer, UK Catapult, explains the strategy
Register now: Lab Innovations celebrates Year of the Periodic Table
Event in Birmingham will feature 35 hours of educational CPD-accredited seminars and the Cleanroom Hub in partnership with <em><a href='http://www.cleanroomtechnology.com'>Cleanroom Technology</a></em> magazine
Procurement and GMP: A conflict in objectives?
A deeper understanding of the unique requirements and the underlying GMP guidelines is essential for purchasing in the pharmaceutical industry. Axel H. Schroeder of Concept Heidelberg, explains
Jim Polarine | STERIS Senior Technical Service Manager
Either chasing tornados or identifying microbial contamination, Polarine travels the world coaching how to put science into action. In this interview, he unveils what a good contamination control strategy looks like
RABS, isolators and the track-and-trace trend
Traditional aseptic production lines are a thing of the past. Isolators are being integrated with traceability systems to watch over safety of the product and the staff. Jorge Nuero of Telstar explains
Think before you wipe
There is no one-size-fits-all for wipes. Understanding facility priorities, material makeup and absorbency is essential to choosing the right one for the task, says Emily Peck of MicroCare
Butterfly valves: Containment and monitoring for API transfer
Michael Avraam of Chargepoint Technology writes about systems that are critical to preventing HPAPIs harming staff and the bottom line
Europe market report: Playing the waiting game
Demand for cleanrooms, products and services is on the rise in Europe despite Brexit uncertainty. Players in the region say biopharma and the new GMP Annex 1 requirements are key drivers of growth
Grant Merrill | AES Clean Technology CEO
Looking back on 25 years in the business, the mechanical engineer spearheading AES tells CT about the strategy moving the company to pole position in the market
Guide to commissioning and qualification
The specific steps companies should follow to complete a cleanroom project, be it a new build or upgrade, are explained in this guide by Mack Powers, Integrao President
GMP Annex 1: A new dawn in cleanroom garment selection
The new set of guidelines will compel manufacturers to change their approach to contamination control including the way they think about cleanroom apparel, as Jean-François Teneul, Life Sciences Market Leader, DuPont, explains
Factoring the uncertainties in cleanroom design
Align your furniture selection to company culture, SOP and continuous improvement if you plan to make your cleanroom fit for purpose, says Sue Springett of Teknomek
A systematic approach to indoor airflow in operating theatres
Research underway in Germany seeks to identify the optimal indoor airflow to employ during surgeries that prevent the risk of infection. Benjamin Zielke, Valeria Hofer, Hansjörg Rotheudt, Anne Hartmann, and Martin Kriegel, explain
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Trending Articles
Harmonisation of Annex 1 and ISO 14644-1: A deeper look
Alexander Fedotov from Invar explains that the harmonisation of standards seems to be a driving force for setting particle limits and why this may not always result in logical scientific decision making
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Must cleanrooms always run at maximum airflow?
Mona Åkerholm and Hannu Nurminen from Elomatic walk through how companies should be rethinking cleanroom ventilation in the age of sustainability and soaring energy costs
EXCLUSIVE: The journey to create Staubli's new robot for pharmaceutical manufacturing
Julien Lora from Staubli talks to Sophie Bullimore about the development of the company's new robotic pharmaceutical solution, discussing the complexities of its launch as well as the pharmaceutical landscape it is launching into
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
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
Upcoming event
ISPE Singapore
19-21 August 2026 | Conference and exhibition | Singapore
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