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March 10, 2023
Webinar Date/Time: Thu, Apr 6, 2023 11:00 AM EDT
February 17, 2023
Day One, Monday, March 13, 2023
Day Two, Tuesday, March 14, 2023
Day 1: 10:00 am – 4:30 pm EST
Day 2: 10:00 am – 4:30 pm EST
January 24, 2023
The scope of data integrity is shown by the data integrity model, which sits within the overall pharmaceutical quality system of a regulated laboratory.
October 07, 2022
A snapshot of key trends and developments in data handling according to selected panellists from the chromatography sector.
October 01, 2022
The term orphan data is used frequently in the context of data integrity. What does it mean for chromatography data systems? How can we prevent or detect orphan data?
August 01, 2022
What do the draft publications ICH Q2(R2) and Q14 for analytical procedure validation and development mean for a regulated GMP laboratory?
April 01, 2022
Our annual review of new high performance liquid chromatography instruments, mass spectrometry systems, and data processing software.
February 01, 2022
A balance printout is a fixed record, and is also called static data. But how static are static data when the weight is used in a chromatographic analysis? Also, have some regulatory data integrity guidance documents failed to comply with their own regulations?
December 01, 2021
Are we ready to let software and instruments take over the art of separations?
February 01, 2021
In September, the World Health Organization (WHO) issued a new guidance document on Good Chromatography Practices. What guidance does it contain and is it useful? Has the document failed its system suitability test (SST) acceptance criteria?