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Market Reports
DACH cleanroom market report: A look at drug pricing, AI impacts, and consolidation trends
Sophie Bullimore examines some of the major global forces influencing the cleanroom facilities being built in the DACH region, and how the design and construction suppliers are reacting
Opinion: Is pharma going quiet on sustainability and why it matters
Keith Beattie from pharmaceutical sustainability expert, EECO2, gives his take on the state of sustainability and greenwashing in pharmaceuticals in 2026
The state of automative technologies in biopharmaceutical manufacturing in 2026
Steven Ng and Josh Russell from AST discuss the types of automative technologies that are being realistically implemented in biopharma in 2026
Pharmaceutical production compliance burdens nobody talks about
Carl Andrews from Original Software investigates what FDA guidance and GAMP 5 require of pharmaceutical firms when software used in regulated environments is updated
9 non-negotiables for hygienic cleanroom layout and design
Michelle Locke from Teknomek and Tim Triggs of the Cleanroom Testing and Certification Board-International look at contamination control through the lens of cleanroom equipment
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
Upgrades, monitoring and more: Touring King’s College Hospital cleanrooms
Sophie Bullimore gives the latest on the King’s College Hospital NHS Foundation Trust’s Aseptic Services Unit, and the future of its cleanrooms
Is VR training for pharmaceutical manufacturing a reality? — Founder gives peek behind the curtain
Professor Ivan Wall, a veteran regenerative medicine expert who founded a VR training company for medicine manufacturing, explains what VR training for cleanroom jobs looks like, how effective it is and why it is needed
Automation in IVF cleanrooms
Sophie Bullimore looks at some of the ways automation and AI are being introduced in IVF labs
A practical guide to global medical device regulatory and standards bodies
Sarah Moore from NSF summarises the basics of being compliant in the medical device sector, and what this means for global cleanroom operations
10 common pitfalls in cell and gene therapy facility design, and how to avoid them
Jason Rossi from AST reviews ten common mistakes in CGT facility design, from not being realistic about heat load, to not accounting for process bottlenecks
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
The realities of pharmaceutical onshoring: a CDMO perspective
Hamilton Lenox from LGM Pharma examines the reality of the push for domestic onshoring as a response to global instabilities
Does cell therapy starting material collection require a cleanroom?
R Marriott, K Land MD, and K Dosanjh JD from Vitalant explain common misconceptions when it comes to cell therapy contamination risk
An A-Z of biobased circular plastics
Stefaan Vanhalle from STAXS explains the different types and their characteristics, along with considerations for special packaging requirements in cleanrooms
London Tech Week 2026: Drug discovery acceleration and speedy CFD analysis
Technology leaders from across the world gathered for a week in London to make connections and educate attendees on recent developments
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Trending Articles
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
Automating HEPA filter scans in barrier systems
Syntegon and InfraSolution discuss how the two companies have launched the first system for automated HEPA filter scans in barrier systems. Thomas Kosian and Christian Dorfner explain
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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
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
The acid test: pH measurement of water quality
For decades pH measurement has been the mainstay of water quality testing in cleanrooms and labs. However Mark Bosley, Business Support Divisional Manager, SUEZ Water Purification Systems, outlines some common pitfalls
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