13 May 2026

Smarter Dissolution Testing: Mastering Staging with q-doc

Automate pharmacopoeial staging workflows and gain full control over dissolution data interpretation with q-doc’s integrated, compliant data management.

Dissolution testing is a well‑established cornerstone of pharmaceutical quality control – but interpreting the results can quickly become complex. This is especially true for pharmacopoeial staging, where results are evaluated stepwise – starting at Stage S1 or L1 and potentially progressing through S2/S3 or L2/L3 – with increasing sample sizes and strict acceptance criteria applied at each stage.

What if this process could be simplified?

With q-doc, SOTAX brings structure and clarity to dissolution staging. Integrated workflows guide users through each stage, automatically applying acceptance criteria and ensuring consistent, compliant decisions – without the burden of manual calculations.

For immediate‑release testing, configurable tolerances and built‑in logic support precise, transparent evaluations aligned with USP <711>.

Curious how this works in practice – and how it can streamline your lab operations?

Discover the full details in our latest Application Note.