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SPECORD PLUS series ASpect UV software

Aspect UV

ASpect UV is our most flexible software solution, with various add-on modules depending on your needs. Keep up to date by upgrading to ASpect UV 2.0, enjoy the instrument control possibilities of the SOAP interface, and use our FDA 21 CFR Part 11 Compliance module to achieve GMP compliance.

Software Update

ASpect UV 2.0 delivers a significant upgrade in functionality and connectivity, enabling more advanced data evaluation with an extended formula editor that supports complex calculations across multiple samples. The new SOAP interface module allows seamless integration with LIMS and LES systems, supporting automated workflows and centralized data management in highly regulated environments. Enhanced compliance features, including Active Directory integration and strengthened electronic signature controls, ensure improved data security and readiness for regulated industries. In addition, optimized kinetics measurements, improved usability, and updated pharmacopoeia validations make ASpect UV 2.0 a powerful and future-ready solution for modern UV/Vis laboratories.

SOAP Interface for ASpect UV

Complete external control of your SPECORD PLUS
With the SOAP interface for ASpect UV, SPECORD PLUS instruments can be seamlessly integrated into LIMS systems. Users can start measurements remotely, manage methods centrally, and automatically transfer results into their digital environment. This reduces training requirements, eliminates manual data handling errors, and enables consistent, traceable workflows across the laboratory.

LIMS Integration Benefits​
Integrating SPECORD PLUS instruments into LIMS streamlines workflows by centralizing control and reducing manual tasks.​

Remote Operation Flexibility​
Remote operation capabilities enable teams to perform measurements across multiple locations efficiently and flexibly.​

Enhanced Data Traceability​
The interface ensures consistent data capture and traceability, essential for reliable digital laboratory management.

FDA 21 CFR Part 11 Compliance Module

Fulfill all compliance requirements with the FDA 21 CFR Part 11 Compliance requirements, featuring user management including connectivity to external Identity Providers like Active Directory, flexible signature definitions combined with an enforced principle of dual control, and an audit trail that captures the changes in values.

Order Information

Ordner numberDescription
830-00024-0FDA 21 CFR Part 11 Compliance module (includes functionalities for secure data storage, user management, audit trailing, and electronic signatures)
830-00028-0USP – NF Compliance (supports validation of SPECORD PLUS instruments acc. to the current United States Pharmacopoeia, chapter <857>).
830-00026-0Ph. Eur. Compliance (supports validation of SPECORD PLUS instruments acc. To the current European Pharmacopoeia).
830-00030-0AJ Compliance (an additional validation module for SPECORD PLUS instruments that makes sure the instrument can be validated to our standards.)
830-00032-0SOAP Interface (enables control of SPECORD PLUS instruments via a SOAP interface)

Downloads

[Translate to English (US):] Flyer UV/Vis Automation Solutions for Industries with High Documentation Requirements (SOAP Interface) (EN)

Open PDF

[Translate to English (US):] Infographic SOAP Interface SPECORD Plus (EN)

Download file

[Translate to English (US):] Flyer UV/Vis FDA 21 CFR Part 11 Compliance (EN)

Open PDF

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