For Head of Analytical / QC
Spectra and purity questions pile up, and sign-offs wait.
This is how it runs today, and how it runs with reproducibly calculated results and a report your expert signs off.
Today and with CovaSyn
Today
- The spectrum comes off the instrument, assignment happens by hand.
- Unknown peak: literature, databases, ask a colleague, wait.
- For a new separation the HPLC method is tried out, not predicted.
- Sign-off waits for the one person who holds the analysis in their head.
With CovaSyn
- You send the spectrum, assignment and purity come back in a report for your review.
- The unknown peak is checked against formula prediction and fragment annotation.
- Column, gradient and expected retention time arrive as a proposal before the first sample runs.
- Every evaluation records input, method version and result; sign-off reviews instead of reconstructing.
What you get is a report that an expert reviews and releases. The decision stays in the lab.
What we evaluate for you
NMR assignment and structure check
NMR analysis (1D + 2D), assignment, purity, batch identification, SST.
Molecular formula from accurate mass and impurity profile
Mass spectra, formula prediction, fragment annotation, impurity profiling.
IR identity check
IR spectra, identification, batch processes, quality check.
UV/Vis content and dissolution
UV/Vis quantification, dissolution, bioanalytics, auto-analysis.
HPLC starting method with column, gradient and retention time
HPLC method development: column selection, gradient, retention time.
Next step
Check it on your own case.
30 minutes on Microsoft Teams. Bring a real spectrum or a separation problem, and we tell you whether and how we can help.