The final decision would usually rest with your customer, and what they have specified with regard to regulatory compliance.
The EP has a general monograph called " Substances for pharmaceutical use" that gives some guidance on the tests required.
Under Assay, they say:- " Unless justified and authorised, contents of substances for pharmaceutical use are determined. Suitable methods are used."
The EP monographs use analytical procedures have been validated and approved using EDQM processes, so you can't assume that you can also use single calibration point assays. Your procedure should have been validated using the ICH guidelines.
The EP WWW site also has a free copy of the Techical Guide to the Elaboration of Monographs, which is a useful 69 page document on the EP monographs.
http://www.edqm.eu/medias/fichiers/tech ... nglish.pdf
Bruce Hamilton