GMP Consulting Supports FDA Audits, SOPs, Testing, and GMP Readiness for Supplement Manufacturers IRVINE, CA, UNITED ...
Expert analysis reveals why NSF GMP and ISO 17025 serve distinct roles and how confusing them lead to compliance gaps, ...
Guide covers five core components of 21 CFR Part 111 quality systems, common FDA cGMP violations, and tips for ...
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 ...
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 ...
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 ...
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