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Advanced Regulatory Compliance  Compatible with Validation from PC Software






 Full Support for Pharmacopeia, GLP/GMP, FDA 21 CFR Part 11 and Other Regulations  Validation can be implemented with PC software by using the optionally available UV validation software.
            In addition to simplifying daily inspections, this makes instrument performance checks and records management easier, enabling more
 Instrument Validation Functions Compliant with JP, USP, and EP  secure regulatory compliance.

 This instrument can not only run checks for nine JIS items, but also those stipulated in the Japanese Pharmacopoeia (JP), United
 States Pharmacopeia (USP), and the European Pharmacopoeia (EP). Naturally, the hardware is also compliant with the specifications
 required by each Pharmacopeia. In addition, the check conditions can be saved. As a result, once the conditions are saved, checks can
 be performed easily just by calling them up as needed. Check results can also be saved.






            • Inspection results can not only be printed but also saved to a file, so the   • The user can select confirmation of instrument performance indicators
             results can be called up later for confirmation.   as per JIS K0115 General rules for molecular absorptiometric analysis, as
            • The inspection parameters can also be saved to separate files for   well as the general test methods in the Japanese Pharmacopeia, USP
             periodic and routine inspections, and then called up for use.  and various EP inspections. (Order inspection jigs and reagents
 Main Screen                                                    separately.)
            Support for FDA 21 CFR Part 11, PIC/S GMP Guidelines and Other Regulations and Guidelines
            Ensuring the integrity of data (database management), including the user management, user authority management, and data audit
            trails required for compliance with FDA 21 CFR Part 11, PIC/S GMP guidelines, and other ER/ES regulations, is possible.

            LabSolutions DB UV-Vis or UVProbe / LabSolutions DB System
            The system allows for data management and user management
            with a database. Compliant with ER/ES regulations, the system is
            optimally configured for customers using a PC.
 Parameters Setting Screen
            LabSolutions CS UV-Vis or UVProbe / LabSolutions CS System (Network System)
            The system is optimally configured for customers who want to manage data on a server together with LC and GC data for ER/ES
            compliance.
 Check Results Screen                                Analysis equipment  LabSolutions server
                                    Client PC        room or an office






 During Testing Screen

 Improved Security Functions

 An external control security function has been added to provide more support for
                            Acquisition
 compliance with regulations. Three user authority levels, "Administrator",   controller PC  UV  FTIR  RF  ICPMS
 "Developer", and "Operator", can be set for instrument users.



 Resolution of 1 nm, the Highest in its Class                             GCMS     AA    TOC

 In addition to achieving a resolution of 1 nm, the highest in its class, by using a monochromator with a Czerny-Turner mounting, the   EDX  Particle size
                                                                                     analyzer
 UV-1900i also features a compact, bright optical system. The instrument is more than capable of meeting the wavelength resolution   Combine with Multi Data Registration license to enable
                               LC   GC   LC   GC                      integrated management of these instruments’ data.
 required in the European Pharmacopoeia.
                                                                                                    UV-1900i
 14                                                                                                 UV-VIS Spectrophotometer  15
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