Cleanroom Standards Articles

QuantumClean® & ChemTrace® Show How to Reduce Wafer Fab CoO at SEMICON Europa 2018

QuantumClean & ChemTrace will demonstrate how its ultra-high purity chamber tool part cleaning, proprietary coatings and microcontamination analytical testing can help reduce wafer fabrication Cost-of-Ownership (CoO). Solutions’ information is available during show hours at SEMICON Europa at the Messe München Exhibition Center in Munich, Germany from November 13 — 16, 2018 (booth A4510).

Medical Device Single Audit Program – How Should You Prepare?

To streamline the oversight of manufacturers’ quality systems, and encourage improved product safety on a global scale, the International Medical Device Regulators Forum (IMDRF) has developed the Medical Device Single Audit Program (MDSAP) whereby recognized Auditing Organizations (AOs) conduct a single audit of a medical device manufacturer that satisfies the relevant requirements of various regulatory agencies.

New Modbus Flow Totalizer for Hazardous Applications

SignalFire Wireless Telemetry introduces the ModQ Sentry, a Modbus Flow Totalizer that interfaces with pulse-type inductive turbine (and other) flow meters to provide instantaneous flow rates, accumulated totals and status information. Units are configurable for volume and time settings and offer options to configure the K factor to match the turbine.

ISO Class 4 Microelectronics Cleanroom Completed for NexLogic Technologies, Inc.

NexLogic Technologies, Inc. has announced the completion of its International Standards Organization (ISO) 14644-1 Class 4/10,000 and the equivalent Federal Standard 209E (FS209E) Class 10 clean room as an integral part of its new microelectronics services and manufacturing capability.

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.

AGT Unveils Cleanroom Technology, Energy Efficiency and Fast Build Times to Empower Growers

The Next Generation Greenhouse: AGT Unveils Cleanroom Technology, Energy Efficiency and Fast Build Times to Empower Growers
Sleek, modern structures full of patent-pending technologies such as Natural Earth Air System, oil bath fans and variable daylight control ushers in a new era for greenhouses

Why Modular Cleanroom Construction?

Why Modular Cleanroom Construction? Modular Cleanroom Construction with modular architectural systems can be modified,...

Using Modular Components to Design and Construct a Cleanroom

What is a CACI?

Compounding Aseptic Containment Isolators (CACI) Provides the maximum level of personnel and product protection This...

what is a compounding cleanroom?

Under USP 797 regulation compounding pharmacies are required to compound sterile preparations (CSPs) utilizing a...

Cleanroom Gowning Best Practices

Proper cleanroom garments for cleanroom gowning are designed to trap and prevent human contaminants, such as those generated by the skin and body, or carried in on their own cleanroom garments, from entering the clean environment. The procedures for cleanroom gowning vary somewhat by industry, but in general, they follow a procedure of “donning” (putting on sterile cleanroom garments) prior to entering, and “doffing” or “de-gowning” (removing special cleanroom garments after exiting), similar to the following: