Both the USA cGMP 1 and EU GMP 2 dictate that cleanroom classification must be carried out according to ISO 14644-1. The version of this ISO standard released in 1999 4 was rewritten by a group of ...

Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points per month, manual data transcription and all too frequently ...

The various GMP guidelines and International ISO standards around GMP cleanrooms are complex and often appear to give conflicting advice, leading to confusion and sometimes incorrect interpretation.

Kuka has introduced a cleanroom-certified version of its autonomous mobile robot (AMR), the KMR iisy CR, designed specifically for sensitive environments such as semiconductor and electronics ...

WILMINGTON, Mass.--(BUSINESS WIRE)--DTG, the leading provider of industrial-strength power systems and mobile workstation solutions, today launched the Cleanroom PowerStation. The mobilized, ...

Qosina, a global supplier of single-use components for medical device and life science OEMs, has completed construction of a 1,700-square-foot ISO Class 8 cleanroom. The addition to its ...

A Clean Room, or cleanroom, is a laboratory environment that ensures that airborne particles are maintained at a very low concentration. This room is isolated, actively cleansed, and prevented from ...