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 ...
A one-size-fits-all approach to monitoring practices and results is never appropriate, given the diversity of practice within the pharmaceutical industry. Cleanroom monitoring and classification are ...
Siddarth Sridharan, left, a teaching assistant for ECE 557, helps undergraduate student Michael Barrow use the optical microscope to take images of samples fabricated inside the cleanroom in the ...
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 ...
In line with the exceptionally high particulate and filmic cleanliness requirements that have to be met for high-tech components in an ever-increasing number of industries, acp systems AG has extended ...
WILMINGTON, Mass.--(BUSINESS WIRE)--DTG, the leading provider of industrial-strength power systems and mobile workstation solutions, today launched the Cleanroom PowerStation. The mobilized, ...
Monmouth's Aluminum Modular Cleanrooms help to create a guaranteed ISO-class clean environment within a pre-existing space or room. Each cleanroom is built upon a free-standing aluminum framework and ...