The 8 references without contexts in paper R. Syubaev D., N. Krutikova M., G. Engalycheva N., N. Olenina G., Р. Сюбаев Д., Н. Крутикова М., Г. Енгалычева Н., Н. Оленина Г. (2018) “Вопросы доказательности эффективности и безопасности гомеопатических лекарственных препаратов // Considerations regarding demonstration of efficacy and safety of homeopathic medicines” / spz:neicon:vedomostincesmp:y:2017:i:2:p:98-103

2
Order of the Ministry of Health and Social Development of the Russian Federation of 26.08.2010, No 750n «On approval of rules of expert evaluation of medicinal products for human use, and of the expert commission opinion form». Available from: https://goo.gl/ 0BcLTp (in Russian).
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3
Order of the Ministry of Health of the Russian Federation of 13.12.2012, No. 1041n «On amendments to the Order of the Ministry of Health and Social Development of the Russian Federation of 26.08.2010, No. 750n «On approval of rules of expert evaluation of medicinal products for human use, and of the expert commission opinion form». Available from: https://goo.gl/zCwXKQ (in Russian).
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4
Guidance on preclinical evaluation of medicines. Part 1. Moscow: Grif i K;2012 (in Russian).
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Guidance on evaluation of medicines. V. I. Moscow: Grif i K;2013 (in Russian).
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6
Guidance on evaluation of medicines. V. II. Moscow: Grif i K;2013 (in Russian).
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8
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use. Available from: https:// goo.gl/20sO2J.
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9
Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use. Available from: https:// goo.gl/OHDyqi.
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12
Guideline on the limits of genotoxic impurities. London, 28 June 2006. CPMP/SWP/5199/02, EMEA/CHMP/QWP/251344/2006). Available from: https:// goo.gl/049hig.
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