Zanamivir Impurity-C

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Zanamivir Impurity-C is a pharmaceutical reference standard used in the analysis of zanamivir, an antiviral drug. It plays a key role in quality control, method validation, stability studies, and regulatory compliance. Essential for ensuring the safety and purity of zanamivir formulations.

Zanamivir Impurity-C

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