Start by asking what you are optimising for, because cost per milligram, documentation depth and lead time do not have a common winner.
Publish the method with the result. A comparison without the laboratory named and the submission dates given is not reproducible by anyone.
Compare documentation on a fixed checklist rather than by impression: lot specificity, method section, chromatogram availability, quantified content, water and counter-ion figures, and whether the code is on the vial.
Gradient slope, column chemistry and detection wavelength all affect the reported purity figure, which is why the method section is the part that makes results comparable.
Name the laboratory and the dates or the comparison cannot be reproduced.