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

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

Trending Articles

  1. 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
  2. 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
  3. Fix for sterilising high-viscosity fluids Filtration can be an effective means of sterilising high-viscosity formulations using hydroxypropyl cellulose (HPC). Pall Corporation and Nippon Soda provide guidance concerning the selection of types of filter media and injectable grade HPC
  4. Incubating settle plates: Understanding growth patterns and when things are going wrong Steven Brimble from Cherwell Laboratories discusses why it is important to your environmental monitoring regime to understand growth characteristics of common cleanroom contaminants and how morphology shifts over time on various media
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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

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