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Both priming and repriming are tested under the same SAC conditions (dose collection apparatus, HPLC assay), and the number of actuations required to achieve label-claim dose output is established for the product labeling

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We have chosen to disclose the above explicitly because researchers will encounter the retraction, the Athira/Kawas matter, and the fosgonimeton distinction during literature review and we believe transparent disclosure serves the research community better than omission

Each supplier is reviewed for reliability, documentation integrity, and transparency in testing

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