Market Reports

Andrew Davies | Microgenetics

The Managing Director of biotech start-up Microgenetics is revolutionising microbiology with the use of machine learning and artificial intelligence to provide real-time analysis of environmental monitoring data

What is the scientific approach to cleanroom HVAC design?

Nigel Lenegan of Energy & Carbon Reduction Solutions answered this question at the Cleanroom Technology Conference 2019 and his presentation is now available online

Draft Annex 1: Cleaning and disinfection clarified

The preliminary version of the guidance for the manufacture of sterile medicinal products details core principles for cleaning and disinfection within a holistic contamination control strategy. Although a draft version, it would be prudent to plan validations with these core principles in mind. Contec's Karen Rossington explains

Coverage, buckets, and validation: The secret to mopping floor surfaces

Contec's Dave Nobile on the best practices to render consistent desired outcomes

HVAC cleanroom design calculation explained

Mecart's Charles Lipeles dissects the key considerations to factor in the drawing board

Guide to wash-in-place process in horizontal mixing systems

Modular solutions are proven to reliably fulfil any industry-specific requirements in the pharmaceutical, food, cosmetics, and chemical industries. Sebastian Steinkamp of Lödige provides a step-by-step guide to effective cleaning

Guide to energy-efficient cleanroom projects

New technology and design tools allow for delivering efficient and resilient manufacturing facilities without a cost premium. Matt Harris and Keith Beattie of EECO<sub>2</sub> explain

Debugging the effluent

Effluent decontamination systems are critical to the safe operation of a contained facility. Microorganisms can easily find their way into waste liquids and disinfectants are toxic, so what is the best way to manage it? Astell's Paul Birchmore explains

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

Trending Articles

  1. 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
  2. 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
  3. 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
  4. 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
  5. What is a semiconductor cleanroom sub-fab? The team at Jimmy Lea P/L discusses the unsung hero of hi-tech production, cleanroom sub-fabs, which require a strict design and construction plan

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