Market Reports

Sustainability in the cleanroom: A scientific approach

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?

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

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

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

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

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
Single-use vs permanent transfer solutions: An overview

Single-use vs permanent transfer solutions: An overview

Isaac Giesen from CRL weighs up the options available to manufacturers for material transfer based on upfront cost, labour, flexibility and target market
Biosafety cabinets: How to avoid back pain with daily use

Biosafety cabinets: How to avoid back pain with daily use

Niggles and issues in the upper body can be caused by repetitive and stagnant processes in a biological safety, David Phillips from Thermo Fisher Scientific, explains how proper ergonomics need to be in place to reduce this to a minimum
Integrating “high-voltage leak detection” into automated visual inspection

Integrating “high-voltage leak detection” into automated visual inspection

Leoni Ransmann and Jan Sende from Syntegon Technology talk about visual inspection of product containers like ampoules, which has been the industry standard for decades, and compare it to modern methods being emphasised in documents like the new EU GMP Annex 1
Responding to cell & gene fill-finish and automation scale-up challenges

Responding to cell & gene fill-finish and automation scale-up challenges

Before delving into some technical details of cell and gene therapy manufacturing, it’s worth pausing to reflect on the human stories that drive this innovation. These therapies are not just scientific marvels - they're changing lives
What is needed for building a nutraceutical cleanroom for a yellow mealworm

What is needed for building a nutraceutical cleanroom for a yellow mealworm

Nutraceutical manufacturer, Nutriearth, which makes a product from yellow mealworm, talks about building their production process into a cleanroom
Implementing PUPSIT in biopharma through streamlined solutions

Implementing PUPSIT in biopharma through streamlined solutions

Hasinah Mohammed from Parker Hannifin’s Bioscience Filtration Division addresses some of the challenges and considerations of implementing PUPSIT within biopharmaceutical manufacturing
How to use portable microbial air samplers effectively

How to use portable microbial air samplers effectively

Yoggya De Silva from Cherwell, an AnalytiChem company, discusses common mistakes with this environmental sampling method and how to avoid them
What does EU GMP Annex 1 classification mean for cleanroom furniture and hygiene protocols?

What does EU GMP Annex 1 classification mean for cleanroom furniture and hygiene protocols?

In this article, Michelle Locke, Product and Marketing Manager at Teknomek, takes a closer look at what EU GMP Annex 1 means for cleanroom furniture and hygienic protocols
How to tell if your glove port interface has a leak

How to tell if your glove port interface has a leak

Isaac Giesen from Central Research Laboratories (CRL) gives a run down on the tell-tale signs that your containment solution’s gloves have a leak
10 points to consider before developing a cleanroom project

10 points to consider before developing a cleanroom project

Graham Findlay from Thomas & Adamson, part of Egis Group, gives some top tips to avoid common problems in a cleanroom builds

Trending Articles

  1. What is MTP technology and how does it affect your cleanroom? What does Module Type Package (MTP) mean for life sciences manufacturing in relation to customised medicines, ease of engineering, and regulatory compliance? Reinfried Kößlbacher from Copa Data discusses
  2. Classification vs monitoring: What is the difference? Understanding cleanroom classification and monitoring is critical to production and compliance. To prevent confusion between these two definitions, Hasim Solmaz, Lighthouse Worldwide Solutions, describes common and different points
  3. B.Braun Medical: The journey to a compounding aseptic production unit Paul Bradley reviews the 24-month design, build and validation process that led the company to expand its Sheffield facility with two new Grade B production rooms increasing capacity by 70%
  4. Assessing disinfection rotation at the point of use: Designing a field trial Qualifications required for disinfectants consist of three phases: suspension tests, surface tests and field trials. The first two phases are well-described as either European or US standards, with surface testing against a range of representative surfaces being regarded as providing a more robust challenge than the suspension test. What is not described in any standard is the field trial. Written by Tim Sandle
  5. Cleanroom construction trends to watch in 2025 and beyond Performance Contracting, Inc. has highlighted the emerging trends in cleanroom construction set to shape the industry in 2025 and the years ahead

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