Preview

Regulatory Research and Medicine Evaluation

Advanced search

Quality standards for immunobiological medicinal products - new texts in the State Pharmacopoeia of the Russian Federation

Abstract

Analysis of XI and XII editions of the State Pharmacopoeia of the Russian Federation proved the necessity and relevance of elaborating quality standards for immunobiological medicinal products as well as methods of their control. Assurance of safety and efficacy of this group of medicines could be achieved only by fulfilling the requirements of modern standards of quality and assuming that methods used for assessment of quality parameters of biologicals are adequate and informative. Top priorities addressed during the preparation of the XIII edition of the State Pharmacopoeia of the Russian Federation were: systematization of quality standards for biologicals on the basis of product types and methods of analysis, and harmonization of requirements for quality parameters with those of the leading world pharmacopoeias, primarily with the European Pharmacopoeia.

About the Authors

A. A. Movsesyants
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


V. P. Bondarev
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


Yu. V. Olefir
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


V. A. Merkulov
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


L. F. Shimchuk
Scientific Centre for Expert Evaluation of Medicinal Products
Russian Federation


References

1. Sakanyan EI, Bunyatyan ND, Sakaeva IV. On the question of elaboration of general monographs and individual monographs for the State Pharmacopoeia of the Russian Federation 12th edition. Vedomosti Nauchnogo tsentra ekspertizy sredstv meditsinskogo primeneniya 2012; (1): 50–52 (in Russian).

2. Mironov AN, Movsesyants AA, Bondarev VP, Ozeretskovsky NA, Shimchuk LF. Highlights of elaborating pharmacopoeia monographs for immunobiological preparations. Vedomosti Nauchnogo tsentra ekspertizy sredstv meditsinskogo primeneniya 2013; (2): 57–59 (in Russian).

3. British Pharmacopoeia. British Pharmacopoeia Commission. V. 1–4. 2009.

4. State Pharmacopoeia of the Republic of Belarus. V. 1–3. Minsk: Tsentr ekspertiz i ispytaniy v zdravoohranenii; 2009 (in Russian).

5. State Pharmacopoeia of Ukraine. Kharkov: Nauchno-ekspertny farmakopeiny tsentr; 2012 (in Russian).

6. European Pharmacopoeia 6.0. Strasbourg: Council of Europe; 2007.

7. The Japanese Pharmacopoeia. 16th edition. Pharmaceuticals and medical devices agency. 2011.

8. United States Pharmacopoeia. 34th, 35th edition. United States Pharmacopoeial Convention; 2012.


Review

For citations:


Movsesyants A.A., Bondarev V.P., Olefir Yu.V., Merkulov V.A., Shimchuk L.F. Quality standards for immunobiological medicinal products - new texts in the State Pharmacopoeia of the Russian Federation. The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products. 2016;(2):38-41. (In Russ.)

Views: 1028


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 3034-3062 (Print)
ISSN 3034-3453 (Online)