Issue
Title
Authors
No 2 (2023)
Issues of adapting the text of the European Union rules of good manufacturing practice to pharmaceutical market of the Eurasian Economic Union
Meshkovskiy A.P., Pyatigorskaya N.V., Belyaev V.V., Beregovykh V.V., Aladysheva Z.I., Brkich G.E., Nikolenko N.S., Filippova O.V., Greibo S.V., Nesterkina E.I., Loseva S.A., Marshalova M.M., Eremeev S.A.
PDF
(Rus)
No 7-8 (2018)
Regulatory aspects of marketing authorization of generic and hybrid medicinal products in the Eurasian Economic Union
Niyazov R.R., Rozhdestvenskiy D.A., Vasiliev A.N., Gavrishina E.V., Dranitsyna М.А., Kulichev D.A.
PDF
(Rus)
No 5 (2018)
Issues of recognition of GLP-status of domestic test facilities and trials abroad
Niyazov R.R., Pozhidaeva D.N., Gavrishina E.V., Dranitsyna M.A., Kulichev D.A.
PDF
(Rus)
No 3 (2018)
The question of strengthening the research capacities in drug innovation
Semin А.А.
PDF
(Rus)
No 3 (2019)
Supplies of medicinal products manufactured in the EAEU countries to Russia
Yutkina I.
PDF
(Rus)
No 10 (2018)
The importance of pharmaceutical quality system design at the drug manufacturers in the context of formation of the EAEU pharmaceutical market
Goryachkin V.V., Smirnov V.A., Shestakov V.N., Abramovich R.A., Denisova M.N.
PDF
(Rus)
1 - 6 of 6 Items

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