Hi,

I work in an ISO:17025 accredited laboratory and would like to use Skyline for routine small molecule quantitation.
At the moment I use Skyline mainly for method development, but I would like to push for routine use as we have different suppliers and providing a training for LC-MS data handling for each supplier is time consuming and not very effective.

Do you know if Skyline can comply with such guidelines? I don't know if these points are covered:

• Full audit trails that track data changes, including who made the change, when and why.
• Time-stamped records of all actions taken within the system.
• Secure user access management with role-based permissions.
• Generation of customisable reports (this one should be OK).
• Ability to generate comprehensive documentation required for audits and inspections.
• Export options in standardised formats (e.g. PDF with chromatograms) for traceability.

Many thanks for your help and all the best,

Gioele