Agilent Technologies provides a wide range of laboratory and compliance services for Agilent chemical analysis instrumentation. These services provide you with the evidence you need to meet the requirements of regulatory agencies such as the U.S. Food and Drug Administration (FDA) and the Environmental Protection Agency (EPA), the International Organization for Standardization (ISO) and the Organization for Economic Cooperation and Development (OECD). These services can also help you save time and money by eliminating the need for you to develop your own operating procedures for qualifying Agilent instruments and training laboratory personnel. These services can ensure that the instrument is performing according to the manufacturer's specifications. These services can also help you follow the same operating procedures and produce the same documentation from laboratory to laboratory, worldwide. This can help you achieve consistent and traceable results, as well as improve method transfer. These services can help you reduce the risk of financial loss due to non-compliance. These services can ensure reliable measurements, including traceable data and complete documentation, from sample introduction to final report, for you, your customers and regulatory agencies.
Agilent Technologies offers a range of support services to help laboratories achieve regulatory compliance for their chemical analysis instruments. These services include Installation Qualification (IQ), Operational Qualification/Performance Verification (OQ/PV), and preventive maintenance to ensure reliable measurements and complete documentation for agencies like the FDA, EPA, ISO, and OECD. This manual is written in Italian.
It is recommended after moving the instrument to another laboratory, adding components, or installing hardware/software patches.
It is recommended after hardware repairs affecting chromatographic parameters or any software modification affecting system security.