Market Reports

The pain of change: Could disinfectant suppliers be part of the cure?

The pain of change: Could disinfectant suppliers be part of the cure?

As an industry with safety as the primary concern, the pharmaceutical industry can often seem quite conservative, but should it be? Ecolab's Matt Cokely discusses
What you might miss when planning an in vitro coupon study

What you might miss when planning an in vitro coupon study

Disinfectant validation typically consists of two distinct testing phases; <em>in vitro</em> testing and <em>in situ</em> testing. It is important not to overlook any important considerations for these tests, STERIS' Richard Chai & Dave Shields explain
Using product inspection for quality control in liquid medicines

Using product inspection for quality control in liquid medicines

In liquid pharmaceuticals, the stakes could not be higher: the correct dosage and usage can literally be a matter of life and death. This article looks at how manufacturers and packaging companies in this field can harness product inspection to ensure they produce high-quality liquid pharmaceutical products. Mettler Toledo's Marco Pelka explains
Annex 1: Changes that will hit EM monitoring programmes

Annex 1: Changes that will hit EM monitoring programmes

Since 2017, Annex 1 Manufacture of Sterile Medicinal Products of EU GMP Volume 4 has been undergoing significant revision. In August 2022, the revisions were finally completed, and will become coming into operation in August 2023. But how do these changes change things? Microgenetics' Edward Webber explains
Less haste more speed: cGMP commercial facility design in 2023

Less haste more speed: cGMP commercial facility design in 2023

The advancement of drug development techniques coupled with the need to deliver potentially life-changing therapies to patients efficiently has made the commercial facility design process increasingly challenging. DPS Group's Eric Quarnstrom explains
How to set up a project for handling highly potent products

How to set up a project for handling highly potent products

In this article, three specialists from Litek focus on the field of primary containment that can be achieved with a suitable design of the process under isolator. Written by Javier Alonso Gómez, Alex García and Gastón Ariel Estruch
Interview with MSL Solution Providers' expert microbiologist Carolyn Burney

Interview with MSL Solution Providers' expert microbiologist Carolyn Burney

The Managing Director and microbiology expert talks about her experience validating disinfectants during a pandemic and taking over as Managing Director in its wake
Case study: Using dynamic air control in a cleanroom

Case study: Using dynamic air control in a cleanroom

A real-world utilisation of dynamic air control in a cleanroom, in this case study EECO2's Jamie Young explains how the system works and gives an update on how the regulatory compliance is going on this fascinating landmark project
Cleanroom Technology Conference Singapore: Day one review of the debut event

Cleanroom Technology Conference Singapore: Day one review of the debut event

This debut outing of the event in Singapore for the contamination control sector fulfilled its promise to deliver a high-calibre programme to an international audience. Here is the day one review of what you missed!
Operating a cleanroom: Consuming consumables conscientiously

Operating a cleanroom: Consuming consumables conscientiously

In sterile applications, it is sometimes not possible to eliminate disposables, but this is not a reason to give up. Andy Whittard from Cherwell Laboratories explains that there is a multitude of other ways to improve the sustainability of these processes whilst maintaining the required cleanliness
Interview with Ward Patton from cleanroom system expert Simplex

Interview with Ward Patton from cleanroom system expert Simplex

With a European modular cleanroom launch on the horizon, US-based Simplex Isolation Systems’ Director of Sales talks about trends in the cleanroom design & builds sector and his hopes and plans for the company to respond to them
Automating HEPA filter scans in barrier systems

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
Digital environmental monitoring: catch failures before they happen

Digital environmental monitoring: catch failures before they happen

There are many benefits to a day-to-day digital monitoring process, but how does it deal with a contamination event in the environment. This is where the benefits go from operational efficiency to operational agility explains Toon Lambrechts from MyCellHub
A guide to choosing the best particle sample point location

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
What is happening in the cleanroom market in 2022's DACH region

What is happening in the cleanroom market in 2022's DACH region

A look at the trends and major business deals through Germany, Austria, and Switzerland in a time of great turmoil across Europe
Interview with PathogenDx founder Milan Patel

Interview with PathogenDx founder Milan Patel

The microarray testing company CEO discusses setting up a company and product to penetrate the microbiology testing market. The entrepreneur also dives into the importance of pathogen testing in the cannabis market

Trending Articles

  1. AES Clean Technology's Chris Miller unveils vision for 2025 and the future of the cleanroom sector Sophie Bullimore from Cleanroom Technology interviews the new CEO of AES Clean Technology on his plans for the company and what he sees as challenges and opportunities in the cleanroom sector in 2025
  2. Contamination control in the food industry: Design zoning Over the years a distinct distance can be observed between the worlds of cleanroom-oriented contamination control and the food processing industry. Current developments in detection techniques as well as an increasing understanding of contamination mechanisms open the pathways to more adequate control. Furthermore, hygienic design has been developed to avoid open process steps, reduce accumulation and improve cleanability. Frans Saurwalt from Kropman Contamination Control explains
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    Overcoming the limitations of traditional airlocks Chris Barbieri from AES Clean Technology discusses the challenges of traditional airlocks and how innovations in design and construction approaches can provide an efficient solution that avoids the need for on-site construction
  4. Back to basics: Control your zones The sanitation process varies depending on the industry, but Patricia Sitek from CR Konsulting talks about common ways to categorise areas in a facility from any sector, and some golden rules to follow for them
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    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

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