Validation of computerised systems is a regulatory requirement for both GMP and GLP laboratories. Although computerised system validation (CSV) has been required for over 40 years, the approaches ...
Digital transformation of analytical processes requires suppliers to design and implement audit trail(s) (AT) that are fit for intended use in a regulated laboratory. In addition, second person review ...
Facility-closure sale of equipment from SoCal-based GenVivo opens on Feb. 11. Closing on February 18, the online auction of equipment from GenVivo's GMP manufacturing and clinical-stage QC laboratory ...
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