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Market Reports
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
Precision cleaning explained
Cleaning to perfection is a sophisticated process and yet vital to product integrity. Dr Brent Ekstrand, VP of Science & Technology at Astro Pak, sheds lights on contaminants and the tests performed to measure them
A strategy for wireless monitoring compliant with 21 CFR Part 11
Paul Daniel, a Vaisala regulatory expert, gives tips for best housekeeping of electronics signatures and records
Real-time feedback for smart energy usage
The Intelligent Cleanroom Control System, a brainchild of EECO<sub>2</sub>, delivers real-time optimisation, demand-based control and fail-safe retrofitting. Keith Beattie, Life Science Lead, explains
Air filtration: Advantages of PTFE materials
Air filter media built with PTFE, the synthetic fluoropolymer of tetrafluoroethylene, has many advantages when it comes to air filtration in cleanrooms and PPE. Robrecht Hendrikx, Market Manager for venting and filtration at Japanese manufacturer Nitto, explains
Choosing doors for food processing facilities
Sheree Headspith of Dortek walks through the qualities and requirements for selecting the right set of doors for food processing areas
Biocide and mop: Powerful combination
The two-in-one system brought to the market by Redditch Medical and HydroFlex keeps biocide and mop separated until application point. A game-changer that only users will appreciate, as Phil Brennan explains
Particle-free production for low fault rates
The growing requirements for circuit-board electronics push manufacturers to integrate clean production into existing processes. Geiger, the German injection moulding expert, demonstrates how enclosures provide a cleaner environment for making plastic components
Building blocks for milk powder manufacturing
Aluminium honeycomb core panels are lightweight and yet boast exceptional strength, a characteristic that combined with non-shedding and incombustible properties make them the material of choice for food processing manufacturers. Elliot Reilly of Puracore, explains
A justified process for cleaning and disinfection
Is a separate and distinct cleaning step always needed before disinfection? STERIS' Walid El Azab explains the scientific approach for choosing the appropriate method for cleanrooms and non-contact product surfaces
US market report: Flexing the muscle
Big ticket R&D projects in biopharma are the main driver of business for cleanroom solution providers in the US. The need for particle-free manufacturing spaces adds to the optimism in the market
A recipe for materials handling facility design
Pharma companies planning an oral solid dose production facility are challenged by different options for the layout. Richard Lockwood, Pharmaceutical Business Line Director, Matcon, explains the considerations for a materials handling area
Adopting cleanroom technology for safer medicinal cannabis
PAC's Mitch Walleser explores the building materials in hyper-clean grow rooms improving medical cannabis yield
How-to guide: Pass box qualification
Material transfer equipment plays an important role in minimising contamination risks during the manufacturing process. Industry expert, Jesus Casas, gives an overview of available pass boxes and a step-by-step explanation on how to qualify them appropriately
Particle counter management for better data integrity and reliability
Jason Kelly, VP of Services, Lighthouse Worldwide Solutions, reveals the best housekeeping methods that users of particle counters can apply to help mitigate against loss of data integrity and accuracy
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Trending Articles
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
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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
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
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
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