Data Integrity for infrared and Raman spectroscopy in OPUS

Pharmaceutical industries face extensive regulations by authorities. For GMP or any other Good Practices (GxP) the FDA described the handling of electronic data with 21 CFR part 11.
To support our customers Bruker provides a spectroscopic software that assures that all requirements for full compliance are met.

https://www.bruker.com/products/infra...)

Standard OPUS validation functions:

- Extensive password and access control management
- Automatic system audit trails covering spectra, methods and software
- Original data cannot be deleted or overwritten
- All data (spectra, evaluation, reports) stored in a single file to guarantee data integrity and smart archiving
- All-in-one solution - no additional software needed.

For more information visit us at:

https://www.bruker.com/de/products/in...