Panel session 13:10

Watch the program
13:10 - 14:30

Grand Hall

Eurasian integration in the field of good practices under current geopolitical conditions

Questions and topics for discussion
• Growth of the common EAEU market under the "Strategy 2025" and development roadmaps
• Review of approved key measures and decisions of the Eurasian Economic Commission in 2020-2022
• Identifying common expert approaches for conducting GMP inspections according to the EAEU rules
• Transition to the supranational regulation. Experience of the EAEU member states
• Further issues of integration and harmonisation. Experience of pharmaceutical companies


The Session Partner: PharmEco Group of Companies

Moderator

Alexei Kedrin

Alexei Kedrin

Chairman of the board of Association of EAEU Pharmaceutical Manufacturers

Yelena Denisova

Yelena Denisova

Deputy Director of the Department of Pharmaceutical and Medical Industry Development, Ministry of Industry and Trade of the Russian Federation

Participants

Natalia Chadova

Chinara Mambetalieva

Deputy Director of the Technical Regulation and Accreditation Department of the Eurasian Economic Commission

Natalia Chadova

Dmitry Rozhdestvensky

Head of the Department of Coordination of the Movement of Medicines and Medical Devices of the Technical Regulation and Accreditation Department of the Eurasian Economic Commission

Natalia Chadova

Yelena Lavnik

Head of the Pharmaceutical Inspection Division, Head Office for Quality Control of Medical Care, Medical Expertise, Appeals of Citizens and Legal Entities, Ministry of Health, Belarus

Natalia Chadova

Zhanar Ordabekova

Head of the Pharmaceutical Inspectorate and Integration, Committee on Medical and Pharmaceutical Surveillance, Ministry of Health, Kazakhstan

Natalia Chadova

Madina Sottaeva

Deputy Head of department for inspection of medicines and expertise, FSI "SID&GP" of the Ministry of Industry and Trade of Russia

Natalia Chadova

Mkrtich Shakaryan

Head of the Good Pharmaceutical Practice Department, Emil Gabriyelyan Scientific Center of Drug and Medical Technologies Expertise, Armenia

Natalia Chadova

Tatiana Tumelya

Head of the Republican Control and Analytical laboratory of RUE "Center for Examinations and Tests in Health Service", Ministry of Health of Belarus

Natalia Chadova

Martkul Musaeva

Head of the Single-window System Division, Drugs and Medical Devices Department, Ministry of Health, Kyrgyzstan

Natalia Chadova

Nazi Abdyrasulova

Head of the Good Practices Division, Pharmaceuticals and Medical Devices Department, Ministry of Health, Kyrgyzstan

Natalia Chadova

Natalia Volovich

Deputy Director - Head of the Registration Department, Representative office of Gedeon Richter in Russia

Natalia Chadova

Hasmik Abrahamyan

Director of the Quality Department, Geropharm Group of Companies

Partners

Session content