Cleanroom Best Practices Articles

TSI Introduces New AeroTrak+ Remote Airborne Particle Counters

TSI introduces a new range of AeroTrak®+ Remote Airborne Particle Counters (APCs) for monitoring manufacturing cleanrooms. TSI is so confident about the performance of the new laser technology inside, that all models are covered by an industry-exclusive standard 5 year laser warranty.

Reusable Cleanroom Garments, Are they the best choice?

Alsico High Tech is a global supplier of garments for cleanrooms, clean areas, ESD environments and operating theatres. Alsico hightech develops, produces and supplies high quality cleanroom, clean area and ESD garments to rental companies, end-users and specialised distributors.

EU MDR: The European Union Medical Device Regulation of 2017

If you are a manufacturer, authorised representative, importer or distributor of medical devices in the EU, or a regulatory affairs or quality management professional involved with medical devices, you need to know how to comply.

EP & Clean Tech China 2019

Regulation and standards for “clean plants” have been increasing in recent years as China’s pharmaceutical R&D and production industry develops rapidly. EP & Clean Tech China 2019, hosted by CCCMHPI, UBM EMEA and UBM Sinoexpo, is an annual event of the pharma clean industry, that will blow a strong, new pharma clean wind in Hall N4 of Shanghai New International Expo Centre (SNIEC). Over 100 Chinese and overseas quality clean enterprises will gather on-site, to showcase the latest pharma cleanroom equipment and products, engineering technologies, and solutions, etc.

TSI Introduces New AeroTrak+ Remote Airborne Particle Counters

TSI Introduces New AeroTrak+ Remote Airborne Particle Counters

TSI introduces a new range of AeroTrak®+ Remote Airborne Particle Counters (APCs) for monitoring manufacturing cleanrooms. TSI is so confident about the performance of the new laser technology inside, that all models are covered by an industry-exclusive standard 5 year laser warranty.

EU MDR: The European Union Medical Device Regulation of 2017

EU MDR: The European Union Medical Device Regulation of 2017

If you are a manufacturer, authorised representative, importer or distributor of medical devices in the EU, or a regulatory affairs or quality management professional involved with medical devices, you need to know how to comply.

Single Pass Versus Recirculating Clean Rooms

Single Pass Versus Recirculating Clean Rooms

The decision that will influence the design of a cleanroom air handling system determining the method to use should be made depending of the desired preciseness of your control. If you are controlling temperature and humidity very tightly, you want to use a recirculating system so that once you’ve conditioned that air, you are not letting the conditioned air escape.

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