The 13 references in paper T. Bokovikova N., E. Gernikova P., E. Sakanyan I., N. Bunyatyan D., L. Shishova I., L. Stronova A., S. Manaeva A., Т. Боковикова Н., Е. Герникова П., Е. Саканян И., Н. Бунятян Д., Л. Шишова И., Л. Стронова А., С. Манаева А. (2018) “Отбор проб в современном фармацевтическом анализе // Sampling in modern pharmaceutical analysis” / spz:neicon:vedomostincesmp:y:2016:i:1:p:33-36

1
General Monograph «Sampling of medicines». The State Pharmacopoeia of the USSR. 11th ed. Issue 2. 1990 (in Russian).
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2
The International Parmacopoeia. 4th edition.
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3
United States Pharmacopeia. 35th edition (USP 35-NF30). Îòáîð ïðîá â ñîâðåìåííîì ôàðìàöåâòè÷åñêîì àíàëèçå
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4
European Pharmacopoeia. 8th edition.
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5
British Parmacopoeia.
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6
General Monograph «Sampling». The State Pharmacopoeia of Republic of Belarus. V. 1. Minsk: Tsentr ekspertiz i ispytaniy v zdravoohranenii; 2006 (in Russian).
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7
Federal Law of the Russian Federation ¹ 61-FZ, 12.04.2010 «On Circulation of Medicines» (in Russian).
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8
Resolution of the Government of the Russian Federation ¹ 982, 01.12.2009 «On the approval of a single list of products subject to mandatory certification, and a single list of products, conformity assessment which takes the form of acceptance of the declaration of conformity» (in Russian).
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9
Resolution of the Government of the Russian Federation ¹ 1043, 15.10.2012 «On Approval of the federal state supervision in the field of medicines» (in Russian).
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10
National Standard of the Russian Federation «Rules of production and quality control of medicines». GOST R 52249–2009 (in Russian).
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11
State Standard R 52537–2006. Production of medicines. The quality assurance system. General requirements (in Russian).
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12
The rules governing medicinal products in the European Union. T4. EU rules on good manufacturing practice for medicinal products for human and veterinary use (GMP EU) «Good manufacturing Practice for Medicinal Products for Human and Veterinary Use».
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13
WHO guidelines for sampling of pharmaceutical products and related materials. Annex 4. WHO Technical Report Series. ¹ 929.2005. AUTHORS Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products» of the Ministry of Health of the Russian Federation, Petrovsky boulevard, 8–2, Moscow, 127051, Russian Federation.
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