Good Laboratory Practice is defined in the OECD Principles as “a quality system concerned with the organisational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported”.

The purpose of the Principles of Good Laboratory Practice is to ensure the development of quality test data and to provide a tool to ensure a sound approach of the management of laboratory studies, including conduct, reporting and archiving.

GLP regulations are applicable to these organizations that perform non-clinical, safety or environmental studies intended to support marketing authorizations. GLP regulations are study based.

For more information on compliance management and on how Rescop can support you in addressing IT quality management and GLP requirements, please refer to our Compliance Solutions or Product Suite section of the website.