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 ...
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 ...
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.
Working with dirty or offgassing components in a clean room can be a challenge. Some industrial and R&D applications require ...
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 ...
Purdue uses nanotechnology cleanroom to expand undergrad class, expose students to high-end research
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 ...
WILMINGTON, Mass.--(BUSINESS WIRE)--DTG, the leading provider of industrial-strength power systems and mobile workstation solutions, today launched the Cleanroom PowerStation. The mobilized, ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback