The NanoRam meets all the requirements of Raman spectroscopy, including Chapter * <858> of the United States Pharmacopoeia, 2.2.48 of the European Pharmacopoeia, 2.26 of the Japanese Pharmacopoeia and all the requirements of the Pharmacopoeia of the People's Republic of China for Raman spectroscopy. Raman Handheld Spectrometers help companies comply with PIC/S and GMP directives when it comes to 100% raw material identification. The NanoRam meets all requirements of 21 CFR * 11 and * 1040.10 of the US Food and Drug Administration (FDA) and can play a key role in a device that complies with cGMP (current US Good Manufacturing Practices). Provide comprehensive training and support, including IQ/OQ/PQ/DQ implementation services, and support services in methodology and/or new library development.