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 ...

Revised versions of ISO 14644 adopt changes to sampling procedures and monitoring plans for cleanrooms. The International Organization for Standardization (ISO) published the long-awaited revisions to ...

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 ...

Dublin, July 28, 2021 (GLOBE NEWSWIRE) -- The "Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers" training has been added to ResearchAndMarkets.com's offering ...

High temperatures are not wanted in cleanrooms, however, in the injection molding process they are unavoidable. Research on the influence of mold temperature by laminar clean airflow underlines the ...

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, ...

(Nanowerk News) The Purdue College of Engineering is using the university's advanced cleanroom at Birck Nanotechnology Center (BNC) for the laboratory to expand an electrical and computer engineering ...