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Cleanroom testing
Cleanrooms are engineered spaces used in research and development laboratories and production facilities. To maintain safety and reduce contamination, cleanrooms must maintain a very low concentration of airborne particulates. In order to monitor the air quality of cleanrooms a process called cleanroom testing is enacted. Depending on the purpose of the cleanroom, the air quality standard may differ so, cleanroom testing can be modified to ensure the cleanliness of any cleanroom.
FEB 24, 2022 | 8:00 AM
Date: February 24, 2022 Time: 08:00am (PST), 11:00am (EST) Fume hoods are often the largest consumers of energy in a lab space and are consequent...
NOV 17, 2021 | 11:00 AM
Date: November 17, 2021 Time: 11:00am (PDT), 2:00pm (EDT) The tripartite International Conference on Harmonisation (ICH) Q2 guide on validation of analytical procedures is not new, but it ca...
MAY 27, 2021 | 10:00 AM
DATE: May 27, 2021 TIME: 11:00am PDT A revised version of the USP chapter on Total Organic Carbon (TOC) USP<643> was published recently and will become official on 1 st May 2021. This...
APR 28, 2021 | 11:00 AM
DATE: April 28, 2021 TIME: 11:00am PDT A revised version of the USP chapter on Total Organic Carbon (TOC) USP<643> was published recently and will become official on 1 st May 2021. Thi...
FEB 24, 2021 | 10:00 AM
DATE: February 24, 2021 TIME: 10am PST Automated lab instruments such as liquid handlers and cell sorters are increasingly common in all types of laboratories, driving fast results for labor...
DEC 14, 2020 | 10:00 AM
DATE: December 14, 2020 TIME: 10:00am PST USP chapter <787>, Subvisible Particulate Matter in Therapeutic Protein Injections, became official August 1, 2014 and provides specific guida...
OCT 23, 2020 | 7:00 AM
DATE: October 23, 2020 TIME: 07:00am PDT, 10:00am EDT The FDA’s 21CFR part 11 guidance on the use of electronic records for data retention or submission is clear. With manually implemen...
NOV 05, 2019 | 8:00 AM
DATE: November 5, 2019TIME: 8:00am PSTThe International Committee for Harmonisation issued their recommendations on validating an analytical instrument, ICH Q2, to support users of a...
APR 04, 2018 | 8:00 AM
A recent report by CPhI highlights the pharmaceutical industry drive to improve productivity by improving right first time quality and reducing overhead costs1. Another report indicates that...
FEB 21, 2018 | 8:00 AM
DATE: TIME: ...
SEP 08, 2016 | 8:00 AM
DATE: September 8, 2016
TIME: 8:00am PST, 11:00am EST
The FDA’s 21 CFR Part 11 guidance on the use of electronic records for data retention or submission is clear. With ...
FEB 25, 2016 | 9:00 AM
February 25, 2016, 9:00am PT, 12:00pm ET, 5:00pm GMT
This webinar, presented by one of the US members to the international revision group, discusses how the newly-revised ISO 14644-1 ...
APR 08, 2015 | 7:00 AM
This educational session will focus on some of the new demands in counting particles in liquids, with a focus on the challenges of preparing and sampling protein-based materials. USP has rece...
APR 08, 2015 | 7:00 AM
This educational session will focus on some of the new demands in counting particles in liquids, with a focus on the challenges of preparing and sampling protein-based materials. USP has rece...