This Technical Report, developed by subject matter experts from the global pharmaceutical industry and regulatory agencies, provides the framework and tools necessary to establish a robust data integrity management system to ensure data integrity for paper, hybrid, and computerized systems within the laboratory. It is intended to outline regulatory requirements and expectations, along with best industry practices, to ensure data integrity, to highlight common gaps in laboratory data management practices, and to recommend methods of remediation.
More Standards PDF
PIP VESHP001-EEDS
$62.00 $125.00
OPEI B71.10-2008
$15.00 $30.00
PIP CVS02010-F
$62.00 $125.00
PIP PN03SD1B01
$37.00 $75.00









