Assessment of laboratories, records, facilities, test articles, test systems, facilities, chain of custody
for compliance with GLP regulations
Laboratory evaluation (personnel training and records, مواد, experimental or analytical documentation, إلخ.)
Laboratory facilities (inspection of sample collection, preparation and storage procedures, analytical procedures and raw data audit, QA documentation audit, إلخ.)
Review SOPs for compliance with international standards
Records, reports and record/sample retention
