Recommendations for drafting regulatory documents on immunobiological medicines particularly the section on physicochemical quality characteristics by O. B. Ustinnikova, O. B. Runova, E. V. Velichko

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Methodological aspects of determining molecular mass distribution of dextrans by size-exclusion chromatography for various groups of medicines by R. S. Smirnov, E. V. Ivanainen, A. I. Lutseva, O. A. Vaganova, D. A. Orlov

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