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7/8/2021

How to Improve Ventilation in a Post-COVID World

TSI Product Marketing Manager Erica Vranak wrote an article for gb&d on ASHRAE and post-pandemic IAQ.

7/7/2021

Construction Dust Monitoring - When the Dust Settles Part 3

What can we conclude from the UK's new environmental legislation? Part 3 of a 3-part series of editorials by TSI's Myles Quigley.

6/30/2021

New Environmental Legislation for the UK - When the Dust Settles Part 2

What is on the horizon for the UK's new environmental legislation? Part 2 of a 3-part series of editorials by TSI's Myles Quigley.

6/24/2021

TSI experts author research paper on indoor air quality

TSI experts Amine Koched, Sebastian Schmitt, Torsten Tritscher, Thomas Krinke, and Oliver Bischof have authored a research paper on indoor air quality, published in IOP Science, the Journal of Physics Conference Series.

6/23/2021

When the PM10 dust settles . . .

What is on the horizon for the UK's new environmental legislation? Part 1 of a 3-part series of editorials by TSI's Myles Quigley.

6/17/2021

TSI team at CIPPE 2021

TSI is exhibiting at the 21st China International Petroleum & Petrochemical Exhibition (CIPPE) at New China International Exhibition Center in Beijing.

6/7/2021

MSP’s New Contamination Standards

The lifecycle of a semiconductor manufacturing inspection system starts in research & development, transitions to manufacturing and production once the design is complete, and is then sold to the customer for use in their fab. Each step of this journey requires stringent testing to ensure the inspection tool is functioning properly.

6/3/2021

TSI is part of ECOTECH China 2021

TSI's Beijing team is exhibiting at ECOTECH 2021, China's largest indoor air quality event, from Jun 2-4.

6/1/2021

TSI congratulates the 2021 TSI/Arthur J. Abrams Memorial Scholarship winner

Congratulations to doctoral student Puleng Moshele, winner of the 2021 TSI/Arthur J. Abrams Memorial Scholarship.

5/17/2021

Being Compliant Using More Efficient Testing Methods for Viable Air Testing in Aseptic Cleanroom Environments

GMP compliance requires medical and pharma manufacturing operations to qualify and routinely monitor microbial contamination levels in cleanrooms and clean spaces. Read this new application note highlighting how active air samplers are an essential part of this process and the critical aspects for evaluation of them.