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Market Reports
Opinion: What is the future of robots in cleanroom maintenance and cleaning?
Ryan McClymonds from i-team Global, explores key challenges of cleanroom cleaning and how these prompted the world’s first battery-powered cleanroom floor cleaning range
10 tips to prepare your pharmaceutical cleanroom for a GxP inspection
Tamika Cathey from NSF gives her top tips to pass FDA, MHRA and EU Annex 1 inspections, ranging from conducting a risk assessment to verifying materials and workflows
Designing contamination control into pharmaceutical equipment
Contamination Control Strategies (CCS) demand a holistic approach to personnel, process design, equipment, and environmental controls. Dr Dave Seaward, from 3P Innovation dives into equipment design aspects that make the difference to the entire system
Stick-built vs modular cleanroom: Which is the right choice for you?
Angstrom company, Life Science Solutions, gives a detailed pros and cons list of the ever-important decision
Opinion: What is the future of robots in cleanroom maintenance and cleaning?
Ryan McClymonds from i-team Global, explores key challenges of cleanroom cleaning and how these prompted the world’s first battery-powered cleanroom floor cleaning range
What is happening in the Indian cleanroom market: Schedule M, IPOs, partnerships and more
Sophie Bullimore looks at the shifting regulatory pressures in the Indian cleanroom sector that are catalysing change across the sector
Pharmaceutical manufacturing: Holistic approaches to digitisation and Industry 4.0
Steven Ng from AST explains how to balance capitalising on the advancements in manufacturing environment technology with meeting 2025’s regulatory demands
An A-Z of USP guidelines and best practice in compressed gas monitoring
Blue Thunder Technologies breaks down USP standards, explores key risks, and outlines best practices for maintaining cleanroom compressed gas compliance and audit-readiness
A review of innovations in sustainable cleanroom operations
Nash Mader from Instant Cleanroom Solutions lists the notable sustainability trends and innovations in action in cleanroom projects in 2025
What is the future of automation in closed systems for cell and gene therapy production?
Dave Seaward from 3P Innovation explains why manufacturers in advanced therapies are moving away from manual, laboratory-based processes and toward automated operations on GMP-compliant production equipment
Sustainability in the cleanroom: A scientific approach
Stefaan Vanhalle from STAXS discusses the ways to reduce a cleanrooms environmental footprint, as well as common traps that companies fall into in this effort
Airflow optimisation: What is it and is big pharma on board?
Over-ventilating cleanrooms leads to exorbitant energy bills, Dan Diehl from Aircuity believes the dynamic air control technology now has a firm foothold in the pharmaceutical sector
A comprehensive guide to cost management in cleanrooms
Kjeld Lund from 14644 Cleanroom deep dives into the critical aspects of cost management in cleanrooms, from personnel to construction techniques
Adaptive cleanroom design: How to take a drug from Phase 1 safety trial to commercialisation
Nick Mazzucca, SVP of Business Development at Chrysalis, explores the core strategies for the drug development lifecycle, from modular facility design and open ballroom concepts to the functionally closed processing systems that unlock a cleanroom’s true adaptive potential
Market report: Cleanroom goggles in North America
Canada-based Klaritex’s CEO, Atif Sarfraz, talks to Sophie Bullimore about meeting the challenges and trends in the cleanroom goggle market in North America
Sporicides: Optimal criteria for cleanroom users
In addition to basic chemicals and formulation, there are other criteria that contribute to making something a sporicide. Tim Sandle, in partnership with Ecolab Life Sciences, explains what you need to know
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Trending Articles
Tips for particle concentration compliance under ISO 14644-1:2015
Apply these six steps to make your cleanroom fit for the new standard, says Hasim Solmaz, Lighthouse Worldwide Solutions
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
A guide to choosing the best particle sample point location
Particle counting in pharmaceutical applications can be clearly segregated into one of three categories: certification, qualification and monitoring. Each category requires a different approach as explained by PMS' Mark Hallworth
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Development, validation, and implementation: How to design your pharmaceutical facility disinfection programme
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
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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