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Preparation of Module 1 of the Registration Dossier According to the EAEU Procedure

Vedomosti Naučnogo centra èkspertizy sredstv medicinskogo primeneniâ (Online), 2022-10, Vol.12 (3), p.341-347

Rychikhina, E. M.

2022

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Special Provisions for the Medicines Registration Procedure in Response to Economic Restrictions Imposed on the Russian Federation

Vedomosti Naučnogo centra èkspertizy sredstv medicinskogo primeneniâ (Online), 2022-07, Vol.12 (2), p.214-221

Rychikhina, E. M.

2022

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Analysis of the provisions of national and EAEU legislation regulating pharmaceuticals before and after 1 January 2026

Vedomosti Naučnogo centra èkspertizy sredstv medicinskogo primeneniâ (Online), 2023-12, Vol.13 (4), p.586-600

2023

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Recommendations on the EAEU Marketing Authorisation Procedures to Optimise the Performance of Regulatory Affairs Specialists

Vedomosti Naučnogo centra èkspertizy sredstv medicinskogo primeneniâ (Online), 2023-07, Vol.13 (2-1), p.345-360

2023

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Actions of the Manufacturers of Herbal and Other High-Demand Medicinal Products According to the EAEU Authorisation Procedures: Practical Recommendations

Vedomosti Naučnogo centra èkspertizy sredstv medicinskogo primeneniâ (Online), 2024-04, Vol.14 (2), p.132-137

E. M. Rychikhina

2024

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INFORMATION SYSTEM FOR EXPERT EVALUATION OF MEDICINES INTERCHANGEABILITY

The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products, 2018-06, Vol.8 (2), p.99-102

2018

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Information technologies as a tool of pharmaceutical data management

Vedomosti Naučnogo centra èkspertizy sredstv medicinskogo primeneniâ (Online), 2018-02, Vol.7 (2), p.122-125

2018

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Preparation of Module 1 of the Registration Dossier According to the EAEU Procedure

Special Provisions for the Medicines Registration Procedure in Response to Economic Restrictions Imposed on the Russian Federation

Analysis of the provisions of national and EAEU legislation regulating pharmaceuticals before and after 1 January 2026

Recommendations on the EAEU Marketing Authorisation Procedures to Optimise the Performance of Regulatory Affairs Specialists

Actions of the Manufacturers of Herbal and Other High-Demand Medicinal Products According to the EAEU Authorisation Procedures: Practical Recommendations

INFORMATION SYSTEM FOR EXPERT EVALUATION OF MEDICINES INTERCHANGEABILITY

Information technologies as a tool of pharmaceutical data management

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