Market Reports

What is happening in the Indian cleanroom market: Schedule M, IPOs, partnerships and more

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

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

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

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?

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

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

Trending Articles

  1. 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
  2. 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
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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
  4. 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
  5. 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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