This is a required field.
Invalid
Part number
Error in validation!

Spectral Analysis Software:
AP Spectroscopy Suite

  • Cora 5001 Direct Raman spectrometer on the left and Cora 5001 Fiber Raman spectrometer with a connected probe on the right, displayed alongside a central monitor showing the Spectroscopy Suite
  • Two laboratory technicians working with an Lyza 3000 FTIR spectrometer placed on the bench in front of a central monitor displaying the Spectroscopy Suite spectral analysis software
  • Cora 5001 Direct Raman spectrometer on the left and Cora 5001 Fiber Raman spectrometer with a connected probe on the right, displayed alongside a central monitor showing the Spectroscopy Suite
  • Two laboratory technicians working with an Lyza 3000 FTIR spectrometer placed on the bench in front of a central monitor displaying the Spectroscopy Suite spectral analysis software
  • +5
Model:
  • Control of Cora 5001 (Raman) and Lyza 7000/3000 (FTIR) from a PC
  • Chemical identification of samples within seconds
  • Convenient method development and spectral processing
  • Lifetime data integrity and audit trail with search function
  • Transparent and secure electronic signing and versioning 
  • Made for pharma compliance
  • Pass audits with lifetime data integrity and a searchable audit trail
  • Ensure trusted results via electronic signatures
  • Perform complex FTIR and Raman spectroscopy tasks with ease
  • Transfer approved results to LIMS and ERP via AP Connect

Perform chemical identification, verification, and quantification of substances using Cora 5001 and Lyza 3000/7000 in seconds, with Anton Paar’s spectral analysis software: AP Spectroscopy Suite. 

The ideal solution for incoming goods inspection, quality control of final products, and R&D in both regulated and non-regulated environments, AP Spectroscopy Suite takes all the complicated spectroscopy aspects out of daily measuring routines. Predefined workflows and settings – designed to adhere to stringent internal and external compliance regulations – speed up analysis and prevent operator error. Methods, reference data, and libraries are thoroughly versioned and can be configured for review and approval using electronic signatures.

Key features

Increase confidence in your QC results

Perform consistent identification, verification, and quantification with controlled user access and guided workflows. Role-based permissions guarantee that only approved workflows are executed, keeping daily sample analysis consistent and secure while minimizing human influence on results. 

The spectral analysis software automatically compares measured spectra with your in-house libraries, Anton Paar’s validated substance libraries, or optional third-party databases for clear identification and verification results. For quantitative analysis, validated calibration models deliver precise concentration values. 

Clear pass/fail decisions or numerical results are generated automatically, minimizing interpretation errors. Strict versioning of methods and libraries increases transparency and ensures that only the latest approved workflows are applied.

Simplify your daily routine with predefined methods

All sample-specific measurements are executed through predefined, method-based workflows. Each method defines sample-specific acquisition parameters, analysis steps, processing routines, and reference data, enabling everyday operators to achieve high-quality results – even for complex spectroscopy tasks. Methods can only be created or changed by user groups with the corresponding privileges. Each method is automatically versioned and can also be configured to undergo a guided review and approval process using electronic signatures, ensuring that only approved methods can be used in the AP Spectroscopy Suite for analysis.

Easy reference library generation

As with the methods, reference datasets can only be generated by users with the rights to do so. Carefully maintained reference libraries for a variety of substance classes are supplied by Anton Paar but can also be created by the user or imported from existing spectrometers, even from other vendors. Overlaying multiple spectra assists in selecting the right reference datasets. Configurable review and approval processes ensure that only approved substances enter a library and that only approved libraries can be used for analysis with the spectral analysis software. Reference substances can also be easily created from historic measurements. Relevant substance metadata, such as CAS numbers and GHS information, completes the reference library.

The best choice for spectroscopy in regulated environments

With AP Spectroscopy Suite Premium, all actions and data are traceable and searchable, helping you pass audits in regulated environments. Functions such as access control via Active Directory (including user group sync), electronic signing, user role administration, audit trail, data management, export, backup, and restore ensure compliance with 21 CFR Part 11, GAMP 5, and EU GMP Vol. 4 Annex 11. Anton Paar’s Analytical Instrument and System Qualification Package (AISQ+) minimizes the effort and time needed to prepare for go-live.

Combined spectroscopy power

Both FTIR and Raman molecular spectroscopy methods can be controlled using the same spectral analysis software. You can use AP Spectroscopy Suite either as Raman analysis software or FTIR analysis software, or combine them for a powerful analytical workstation. Technology-specific features such as checks, adjustments, and corrections are available where needed. The system ensures your instrument is always ready to measure by requiring a valid system suitability test as a prerequisite. Spectroscopy labs only need a single software platform, which streamlines workflows and reduces training requirements.

Specifications

FeatureProfessionalPremium
Target customersSpectroscopy labs with a broad range of applications running Raman, FTIR, or bothSpectroscopy labs operating in highly regulated environments and users with stringent testing requirements
IndustriesChemical industry, universities, R&D, unregulated QC labsPharmaceutical industry, personal care industry, healthcare industry
License modelOne-time license per workstation, with unlimited users and devices; license is transferableOne-time license per workstation, with unlimited users and devices; license is transferable
Methods and libraries
Identification, verification, and quantification
Roles and permissions
Active Directory
Database technologySQLSQL
AP Connect integration
Electronic signature 
Configurable review process 
Audit trail 
Compliant with 21 CFR Part 11 and related regulations 
Data record retentionRecycle bin with deletion/recoveryPharma-compliant archiving with lifetime data integrity
Export formats.csv, .pdf, .spc
User interface languagesEnglish, German, Chinese (simplified), Chinese (traditional), French, Spanish, Italian, Japanese, Korean, Polish, Turkish

Standards

Open all
Close all

CFR

21 Part 11

GAMP

5

EU GMP

Vol. 4 Annex 11.

European Pharmacopoeia (Ph. Eur.)

2.2.24
2.2.48

US Pharmacopoeia (USP)

854
858
1858

Japanese Pharmacopoeia (JP)

2.25
2.26

Chinese Pharmacopoeia (ChP)

0402
0421

IP

2.4.6

Standards

Open all
Close all

CFR

21 Part 11

GAMP

5

EU GMP

Vol. 4 Annex 11.

European Pharmacopoeia (Ph. Eur.)

2.2.24
2.2.48

US Pharmacopoeia (USP)

854
858
1858

Japanese Pharmacopoeia (JP)

2.25
2.26

Chinese Pharmacopoeia (ChP)

0402
0421

IP

2.4.6

Anton Paar Certified Service

The Anton Paar quality in service and support:
  • More than 350 manufacturer-certified technical experts worldwide
  • Qualified support in your local language
  • Protection for your investment throughout its lifecycle
  • 3-year warranty
Learn more

Compatible instruments

Industry
Applications
Standards
Your choice: Reset all filters