Ru | En

Speakers of the Second Russian GMP Conference 2017

Speakers. First Day, September 18

 

manurov

Denis Manturov

Minister of Industry and Trade of the Russian Federation 

Education:

1994 – Lomonosov MSU, majoring in Sociology;

1997 – MSU postgraduate, Candidate of Economic Sciences;

2002 – Doctoral studies at Moscow Aviation Institute;

2006 – Russian Academy of State Service under the President of the Russian Federation, majoring in Law.

Professional activity:

1998 – appointed Deputy General Director at Ulan-Ude Aviation Plant;

2000 – appointed Commercial Director of Mil Moscow Helicopter Plant;

2001 – appointed Deputy Chairman of State Investment Corporation (Gosinkor);

2003 – appointed General Director of OPK Oboronprom;

2007 – appointed Deputy Minister of Industry and Energy of the Russian Federation;

2008 – appointed Deputy Minister of Industry and Trade of the Russian Federation;

2012 – appointed Acting Minister of Industry and Trade of the Russian Federation;

2012 – appointed Minister of Industry and Trade of the Russian Federation.

Awards:

In 2007, received a second-class medal of the Order of Merit for the Motherland;

In 2008, received the Order of Friendship;

In 2009, received the Order of Honor;

In 2010, received a Certificate of Merit from the Russian Federation Government;

In 2013, received a fourth-class Order of Merit for the Motherland.

kondratiev

Veniamin Kondratev

Governor of the Krasnodar Region

Education:

Kuban State University, specialty "Lawyer". Ph.D. in Law.

Career:

From 1991 to 1994 - legal adviser, head of the legal sector of JSC PLUTOS, Krasnodar;

From 1994 to 1995 - senior legal adviser and leading specialist of the legal department of the Administration of the Krasnodar Region;

From 1995 to 2001 - Deputy, First Deputy Head of the Legal Department of the Administration of Krasnodar Region, Head of the Department of Systematization and Legal Expertise of Regulatory Legal Acts.

In 2001-2003, he was deputy head of the staff, head of the legal department of the Administration of the Krasnodar Region;

From 2003 to 2007 - Deputy Head of Administration (Governor) of the Krasnodar Region on property issues, land and legal relations, Head of the Department of Property Relations of the Krasnodar Region;

From 2007 to 2014 - Deputy Head of Administration (Governor) of Krasnodar Region, Head of Property Relations Department of Krasnodar Region;

From 2014 to January 2015 - Deputy Chief of the Main Administration of the Federal Property of the Administration of the President of the Russian Federation;

January 2015 - appointed to the post of Chief of the Main Administration of the Federal Property of the Administration of the President of the Russian Federation;

March 2015 - appointed Deputy Executive secretary to the President of the Russian Federation;

Under the Decree of the President of the Russian Federation of April 22, 2015 appointed temporarily acting head of the Administration (Governor) of the Krasnodar Region;

According to the results of the elections held on September 13, 2015, Veniamin Kondratiev scored 83.64% of the vote and became the elected Governor of the Krasnodar Region;

September 22, 2015, he officially took office as the Head of the Administration (Governor) of the Krasnodar Region.

tsib

Sergey Tsyb

Deputy Minister of Industry and Trade of the Russian Federation

Education:

Graduated from Plekhanov Russian University of Economics cum laude, Ph.D. in Economics.

Career:

1996- General Director LLP "RCC", Moscow;

2000- General Director CJSC "Medbiopharmcentre", Moscow;

2006- General Director LLC "Radiopreparat", Moscow;

2007- Director of the Department for chemical-engineering complex and bio engineering technologies of Minenergo of Russia;

2008- Director of the Department for chemical-engineering complex and bio engineering technologies of Minpromtorg of Russia;

2013- Deputy Minister of Industry and Trade of the Russian Federation.

Awards:

In 2009 he was awarded with lapel pin "Miloserdie";

In 2011 was awarded with reward of the Government of the Russian Federation in the field of Science and Technology for developing and implementing of scientific basis for the creation of a national system for the safe circulation of chemical products.

maksimkina

Elena Maksimkina

Head of the Department of Drug Supply and Regulation of Medical Devices of the Ministry of Health of the Russian Federation

Education:

Graduated from the Pharmaceutical faculty of the First Moscow Medical Institute in 1984.

Career:

Since 1984 she worked at the Institute as a senior laboratory assistant since 1984, assistant (1986-1989), senior lecturer (1989-1993), associate Professor (1993-2005), Professor of Faculty of Organization and Economy of Pharmacy, Faculty of Pharmacy (2005-2006), Head of the Department of Management and Economics of Pharmacy (since 2007), Dean of the Faculty of Postgraduate Professional Education of Pharmacists (from 2005);

A specialist in the field of management and economics of pharmacy, PhD of Pharmacy, Professor;

She is the author of the first dissertation in the field of marketing research in the pharmaceutical market of Russia, one of the founders and editors-in-chief of the professional pharmaceutical journal "LadyVita" (2003-2004);

Since 2005 is editor-in-chief of the professional pharmaceutical journal "Pervyi Stol";

Since 2007 - member of the international pharmaceutical organization FIP;

From July 2013 - Assistant Minister of health of the Russian Federation;

In October 2013, was appointed as Director of the Department of medicine supply and regulation of medical devices circulation, Russian Ministry of Health.

kosenko

Kosenko Valentina  

Head of the Department for Organization of State Control of the Quality of Medical Products of the Federal Service for Surveillance in Healthcare

Education:

Ph.D. in Pharmacy, graduated from the Pyatigorsk Pharmaceutical Institute, the Pharmaceutical faculty, specialty pharmacist - analyst.

Career and awards:

Has experience of teaching, practical experience in managing positions in the control and analytical laboratory, the organization of the manufacturer of medicines, the state civil service;

Awarded with the medal "In memory of the 850th anniversary of Moscow" of the Moscow Region Administration;

Has an honorary title "Honored worker of public health services of the Russian Federation”.

shestakov ok

Vladislav Shestakov

Director of The Federal State Institution "Federal Institute of Drugs and Good Practices" (FSI "SID and GP')

Education:

In 2001 he graduated from the Academy of Labor and Social Relations, specialization “Organizations Management”.

In 2005 he graduated from the State University of Management, specialization “State and municipal management”.

Career:

Since 2003 he has been participating on a regular basis in educational programs for management of commercial and government organizations, as well as specialized programs in the field of pharmaceutics and pharmaceutical production.

Since 2015, he has been certified as a GMP inspector / auditor. He has Russian diplomas on professional retraining in the field of GMP-inspection / audit, international certificates of WHO (GMP-inspection, Quality Management System for national medical regulatory authorities).

He has been working in the field of healthcare and pharmaceutical industry since 1997, he held leading positions in such companies as “Irbit Chemical Plant”, “Fita Line”, “Hemofarm”, “Makiz-Pharma”, “Skopinsky Pharmaceutical Factory”, “Epidbiomed”, “Farm-Synthesis”, “Binnopharm”, “Usolye-Siberian Chemical and Pharmaceutical Plant”, “Nanolek”, “Altayvitamin Trading”.

He was the Chairman of the branch office of the Federal Interdisciplinary Council for Pharmacy of the All-Russian Public Organization “Delovaya Rossiya” (“Business Russia”), Deputy General Director of the FSI “Federal Center for Industrial Development Assistance”, GR Director of the NGO “Union of Professional Pharmaceutical Organizations”, Co-chairman of the Interdepartmental Commission for the development of a strategy for the medical industry of the Government of the Russian Federation.

From 2013 to the present time he is the Director of the Federal State Institution “State Institute of Drugs and Good Practices” (FSI “SID & GP”) under the Ministry of Industry and Trade of the Russian Federation (formerly FSI "SIB and M").

In 2016 he was appointed as Deputy Head of the State GMP-inspectorate and elected as the Head of the Committee on Good Practices of the Council on Professional Qualifications in the Field of Pharmacy of the National Pharmaceutical Chamber.

olefir

Yury Olefir

PhD in Medicine, General Director of FSBI "Scientific Centre for Expert Evaluation of Medicinal Products" of the Ministry of Health of the Russian Federation 

Education:

Graduated from the Military Medical Academy named after S. M. Kirov cum laude in 1984, in 1989 Residency of the same Academy on a specialty "Urology", furthermore in 2008 received specialty "Health Organization and Public Health" in the Russian State Medical University of Roszdrav.

Career:

1984-1987 — Chief Medical Officer on atomarine of Northern Fleet. Participant of 5 stand-alone navigations.

1987-1989 — Resident of Urology Faculty of Military Medical Academy named after S. M. Kirov.

1989–2008 — military medical service in Central Military Clinical Aviation Hospital No 7 (Moscow) in positions of Junior and Senior Research Assistant, Senior Registrar, Head of Urology Department, Head of Urological Centre – Leading Urologist of the hospital. Doctor of Higher Category in specialty "Urology". Distinguished doctor of the Russian Federation. Retired Colonel of Medical Service.

2008 - Chairman of the Committee on Public Health of the Novgorod Region.

2008-2009 - Minister of Health of Irkutsk region.

2010-2012 - Advisor to the Governor of the Samara region.

2012-2013 - Deputy General Director of RT - BIOTECHPROM.

2013-2015 - General Director of RT - BIOTECHPROM.

Since April 8, 2015 - Acting General Director of FSBI "Scientific Centre for Expert Evaluation of Medicinal Products" of the Ministry of Health of the Russian Federation.

Since November 3, 2015 - General Director of FSBI "Scientific Centre for Expert Evaluation of Medicinal Products" of the Ministry of Health of the Russian Federation.

Scientific activity:

Doctor of Medicine, scientific rank - senior research associate, author of 220 publications, 3 inventions, trained 4 PhDs.

Awards:

He was awarded the Order of Honor, medals: "70 Years of the Armed Forces of the USSR", "300 Years of the Russian Fleet", "In Memory of the 850th Anniversary of Moscow", Zhukov and other departmental Soviet and Russian medals.

kulikov

Ivan Kulikov

Head of the Department of Industrial Policy of Krasnodar Region

Education:

He graduated from Irkutsk State University with a degree in "Management of the organization", qualification "manager".

In 2008 I.A. Kulikov defended his thesis on the topic: "Organizational and economic development of airport facilities". In 2009, by the decision of the Dissertation Council of the State University of Management (Moscow) Mr. Kulikov was awarded the degree of Candidate in Economics.

Career:

Mr. Kulikov has experience working in the economy sector - since 2002 he worked in senior positions at the enterprises of Irkutsk.

From 2008 to 2011 Mr. Kulikov worked in leading positions in the Ministry of Economic Development of Irkutsk Region.

In April 2011, by the order of the Head of Administration (governor) of Krasnodar region Mr. Kulikov was appointed the First Deputy Head of the Department of Investments and Project Support of Krasnodar Region. Later, he held senior positions in the Ministry of Strategic Development, Investments and Foreign Economic Affairs of Krasnodar Region, and in the Ministry of Economics of Krasnodar Region.

In December 2015 Ivan Kulikov was appointed Deputy Minister of Industry and Energy of Krasnodar Region.

Since January 2016, he had been acting as the Head of the Industrial policy department of Krasnodar Region.

In April 2017 he was appointed the Head of Industrial Policy Department of Krasnodar Region.

cheskotti

Oliver Cescotti

President of Group of Companies GEA in Russia, Kazakhstan, Belarus, Central Asia and the Caucasus

Education:

Political science in West Berlin and Munich.

Career:

From 2006 Mr. Cescotti had been managing one of the subsidiary companies of AO GEA Group and had been responsible for development the direction of industrial cold and gas compressors in the food, chemical, oil and gas, and energy industries. In 2015 Oliver Cescotti became the Head of all subsidiary companies of AO GEA Group in Russia. Currently he is responsible for consolidation of all the companies into one legal entity. Moreover, Mr. Cescotti is supplementary responsible for all the sales and projects realization on the territories of Russia, Belarus, Kazakhstan, Central Asia and the Caucasus.

One of the key directions is the development of service, in which 30 % of staff members in Russia are involved. In 2015, upon the initiative of Oliver Cescotti, a multifunctional assembly site was set up in Moscow region, Klimovsk, with the area of 2500 square meters. Here, plants for the food, chemical and oil and gas, and energy sectors are assembled, including installations of stainless steel for the food industry. In the future it is planned to expand production for equipment and installations for the food and pharmaceutical industries with a high level of localization.

sharonov

Aleksandr Sharonov

Technical Director ZETA OOO

Education:

University of Chemical Technology of Russia named after Dmitry Mendeleev, Ph.D. in Chemistry.

Career:

Alexandr Sharonov has more than 19 years of experience in pharmaceutical industry. He worked in the top Russian, European and international engineering companies (Chistyi vozduh, Pharmaplan, PharmaGroup, PM Group, ZETA) as an expert and project manager for designing, equipping and qualifying new and reconstructing existing pharmaceutical productions of various types. Member of ISPE since 2007. Specialization - design and engineering in the field of solid dosage forms, sterile and non-sterile liquid medicines, technological design and design of R & D and QC laboratories design.

Skills:

Pharm engineering, Project management, Qualification and validation, Multi-office project execution.

Professional experience:

STENTEKS LLC, Russia, New Construction, Conceptual Design, Stage Project. 25,000 m2. Production - medical products (coronary stents, catheters).

VERTEX, Russia, New construction, Conceptual design, Stage Project. 32,000 m2 Production – Solid dosage forms / Soft dosage forms / liquid non-sterile forms, including sex hormones.

TAKEDA (NIKOMED), New construction, Basic design, Detailed design, Plant for the production of injection solutions and solid dosage forms. Yaroslavl, Russia.

FSUE "Moscow Endocrine Plant", the project - "turnkey". Reconstruction of the workshop for the production of injectable drugs using the BFS method.

"Binnopharm", Conceptual, Basic project, plant for the production of injection solutions, pharmaceutical aerosols and solid dosage forms, Complete reconstruction.

State Research Organic Chemistry and Technology, "turnkey" project, Vivarium for laboratory animals, Complete reconstruction.

"ZIO - Health" Production of Solid dosage forms, New Plant, Russia.

Petrovax Lab, Pilot production of substances for injection, Moscow, Russia.

LLC "Biocom", the project - "turnkey". Production of solid dosage forms, Stavropol, Russia.OOO MAKIZ FARMA, Manufacture of solid dosage forms, Moscow, Russia.

kukava 1

Kukava Vadim

Executive Director InPharma

Education:

International University in Moscow, law faculty.

Career:

From 2004 to 2006, Vadim worked as a specialist at the Federal Agency for State Property Management. He had a diverse range of responsibilities with respect to relations between the Russian Federation, as the State owner of the forest and chemical industries.

From 2006 to 2009, Vadim Kukava worked in the corporate relations department of a large international FMCG company. He was responsible for interaction with the Government and the professional industry communities.

From 2009 to 2012, Vadim Kukava worked as a Public and Government Relations Manager in a large international company specializing in the production of timber industry products, medical devices and hygiene products. Vadim established this position, as well as all ley initiatives in the Russian division of the company. He was responsible for interaction with public authorities, professional associations and unions of patients. Vadim actively participated in industrial associations, including the Association of Perfumery, Cosmetics and Household Products (as a member of the Board), and the Association of International Manufacturers of Medical Devices IMEDA.

In 2012, Vadim Kukava was invited to the position of Executive Director of the Association of the world's leading innovative pharmaceutical companies InPharma.

zdeneka

Zdenek Pavelek

Director of the Department of Quality and Training FAVEA Group

Education:

Masaryk University in Brno (Czech Republic), faculty of natural sciences.

Career:

Prior to joining FAVEA, Zdenek worked as a Director of the quality management department at TEVA Czech Industries.

He also previously held the position of Head of Quality Control at Galena.

During his work Zdenek Pavelek has developed a number of author's training courses and lectures for the training of specialists of pharmaceutical companies in the Czech Republic and other European countries (Slovakia, Poland, Latvia, Lithuania, Germany, Switzerland), as well as Ukraine, Russia, Kazakhstan, China and Brazil. Zdenek also has extensive experience in the validation of analytical methods, validation processes, purification validation, equipment qualification and computer system validation.

Currently, he actively participates in the preparation of pharmaceutical manufacturers of medicines for oficcial controls and audits be EU and US regulators, and also deals with Quality Management of FAVEA projects.

merck 2

Najib Sehat

Head of Global Regulatory Management, Life Science

Education:

Sehat has a Diploma, Ph.D. in Chemistry and German State Board Certification in Food Chemistry. He has resided in 3 continents (Europe, North America and Asia) and highly values these experiences.

Career:

Najib Sehat is Head of Global Regulatory Management for the Life Science business of Merck. In this role, he is responsible for all regulatory activities worldwide for the diverse Life Science portfolio and the entire life cycle management. These activities include the registration and licensing of products, import and export permits and related site registrations as well as strategy and concept development for registration of aforementioned products. His role requires proactive surveillance of the ever-changing global regulatory landscape and the expertise to meet new or changing regulations.

Sehat joined Merck in 1999 and has almost 20 years of experience in regulatory, quality and technical service leadership roles within Merck. This includes expert knowledge for regulatory & quality requirements for the diverse Life Science portfolio. Prior to joining Merck, Sehat’s work experience includes five years with the U.S. Food and Drug Administration in Washington, D.C. and three years employed with Hamburg University and the Hygiene Institute in Hamburg, Germany.

paroshin

Oleg Paroshin

General Director LLC Amgen (Russia)

Education:

Russian National Medical University, Pediatrician. Magdeburg University, MBA: International Management. INSEAD: "Leadership Programs for General Directors". INSEAD: "Leadership Development Program for Senior Managers". INSEAD: "Corporate Strategies (Finance & Law)". INSEAD: "Competition Strategy". BIO-Europe: "Advanced Business Development Course".

Career:

2001-2003 - worked as a Medical Advisor / Access Manager at Jhonson & Jhonson.

Since 2003, he led the Business Unit for CIS (Kazakhstan and Central Asia).

From 2006-2007 he headed the Department for work with key customers and the Supply Department at UCB Pharma.

Since 2007, he held executive positions in Amgen Company (Key Account Manager, Key Account Managers Lead, Access Director, Commercial Director).

Since 2014 - General Director of LLC Amgen (Russia).

Since the appointment of O. Paroshin General Director of LLC Amgen (Russia): Amgen products entered the top 10 most wanted biological products according to IMS, the company won one of the most prestigious international pharmaceutical prizes - Prix Galien Russia, and also won an independent contest for the title of the best employer, and became the owner of the world award Best Employer.

novikova

Irina Novikova

Executive Director of the Association "Kaluga Pharmaceutical Cluster"

Education:

Graduated from the State University of Management, specialty "Financial Management", postgraduate study at the State University of Management, Ph.D in economics. Passed professional retraining in the specialty "Marketing" in the Moscow International Business School "MIRBIS". Advanced training: the Swedish Management Institute, California State University Fullerton (USA), the University of Applied Sciences of Jyväskylä (Finland), the Higher School of Economics (Moscow) under the programs of formation and development of clusters, financing innovative projects, project management.

Career:

Since 2015 - Executive Director of the Association "Kaluga Pharmaceutical Cluster".

Since 2010 - Deputy General Director of JSC "Agency for Innovative Development - Center for Cluster Development of the Kaluga Region".

Member of the working group "Effective management of territorial clusters" of the Ministry of Economic Development of the Russian Federation and JSC "Russian Venture Company." Experience in the non-state sector for more than 15 years. Author of more than 30 scientific articles and reports on grants. Co-author of the monograph "Territories of Innovative Development".

rozhdestvenskiy

Rozhdestvenskiy Dmitriy

Eurasian Economic Commission, Department of Technical Regulation and Accreditation (Russian Federation), Head of the Coordination Department in the sphere of circulation of medicines and medical products

Education and professional activity:

1998 - UO "Vitebsk State Medical Institute".

1999-2002 - Postgraduate studies, then clinical residency of Vitebsk State Medical University, specialization in Clinical Pharmacology. 2002-2004 - Department of General and Clinical Pharmacology of Vitebsk State Medical University (Republic of Belarus).

2002-2004 Department of General and Clinical Pharmacology ofVitebsk State Medical University (Republic of Belarus).
2004-2014 - Republican Clinical-Pharmacological Laboratory of the UP "Center for Expertise and Testing in Health Care" (Republic of Belarus).

2014-untill now - Eurasian Economic Commission, Department of Technical Regulation and Accreditation (Russian Federation).

Area of practical interests:

Clinical studies of medicines, biological statistics, clinical pharmacology.

Research work:

Planning, implementation and quality assurance of more than 140 bioequivalence studies of reproduced (generic) medicines in the Republic of Belarus, 30 clinical trials of pharmaceuticals (allergology, cardiology, neurology, ophthalmology) of I and III phases.

chagin

Dmitriy Chagin

Board Chairman of Association of Pharmaceutical Manufacturers EAEU

Education:

In 1989 graduated from The S. M. Kirov Military Medical Academy a degree in "General Medicine". In 2002 took a training course on the topic "Local government: problems and development trends".

Career:

Since 2011 till now he has been working as Director of Alliance in the sphere of design, manufacturing and circulation of medicines and medical devices “Medical-pharmaceutical projects. XXI century”.

January,1st, 2016 till now he is a Chairman of the Board of the Association of Pharmaceutical Manufacturers of the Eurasian Economic Union, which united the majority of innovative companies in the field of research, design and production of pharmaceuticals of the countries of the Eurasian Economic Union (Republic of Armenia, the Republic of Belarus, the Republic of Kazakhstan, the Kyrgyz Republic and the Russian Federation).

chadova

Natalia Chadova

Head of Drugs Manufacturing Inspecting Department of FSI "SID&GP"

Education:

Lomonosov Moscow State University, Candidate of Chemical Sciences, Production management, MBA - production management, qualification upgrade in GMP/GDP Inspection/Audit.

Career:

In 1997 moved from Scientific Laboratory to the production. During 9 years she was working at Moshimpharmpreparaty, From workshop technologist to Deputy General Director for Production and Technical Affairs. March 2006 – July 2010 - CJSC «Binnopharm» («MTH»), Management of realization of pharmaceutical production construction (including vaccines) from the concept stage. October 2010 – October 2015 - CJSC "PharMedica" (Engineering Company). From October 2015 – Head of Pharmaceutical Production Inspection Department.

fedegari

Giuseppe Fedegari

President of Fedegari Autoclavi SpA

Education and career:

1980 (Spring) Fedegari Autoclavi SpA opens a manufacturing facility in southern Switzerland (Canton Ticino) for assembling approx. 2000 sterilizers for the German Army (Bundeswehr) and German Civil Protection and the whole family moves to Lugano.

1980-84 Attends high school (Lyceum Alpinum Zuoz) in Switzerland in the foreign language section (D Abteilung); being a German speaking school and due to the different school programs, starts 2 years earlier compared to the Italian school plan. Completes the study obtaining the Swiss Federal “Maturity Degree” (64/90 points).

During school, vacation works in Fedegari Autoclavi SpA, mainly doing different jobs in all production areas.

1984 (Spring) returns to Pavia/Italy and starts working full-time in Fedegari Autoclavi SpA, mainly following factory acceptance tests with customers and assisting the sales mgr. in the negotiations with foreign customers, especially with German speaking ones and international distributors.

1984-87 Fall 1984 attends part-time the university in Pavia (faculty of Chemistry & Pharmaceutical Technology) while working.

1987 Stops attending the university because of the involvement in the business (the sales mgr. leaves the company) and lack of interest in the subjects.

1987-88 Replaces on a temporary basis the sales mgr., while the company is selecting the new manager that is hired in fall.

1988-90 Keep working as technical assistant to the sales mgr. with direct responsibilities on German speaking countries. Work 50% of the time with R&D and Engineering, assisting the sales mgr. in offering/negotiating highly customized sterilizers.

1990-93 Retirement of the general mgr. Works to complete the organization of IT department and prepares the work for the adoption of a QA System which is certified in 1994.

1993-00 The company diversify the production in the field of supercritical CO2 plants and the development of the relevant technologies. Works mostly on the new projects/technologies and the improvement of the company information system.

2001 Due to diversification of production an assembling facility for serial-production equipment is opened in Canton Ticino (Switzerland); in this project transfers some commercial competences in the new company.

2007 Coordinates the opening of the 1st daughter company abroad, in the US (Fedegari Technologies, Inc.) with the goal to replace the existing representative who cannot guarantee any further growth of the company in the country and is nominated President.

2008 Works with the brother to open a daughter company in Singapore (Fedegari Asia Pte. Ltd.) through which all Asian representatives are supported.

2010 Coordinates the opening of the German daughter company (Fedegari GmbH) intended to replace the former representative that is not successful any more in selling the industrial equipment and is nominated President.

2015 The Board of Directors nominates him President of Fedegari Autoclavi SpA thus controlling the whole Fedegari Group.

semenov

Alexander  Semenov 

President of CJSC ACTIVE COMPONENT

Education:

Graduated from History Faculty and postgraduate from Faculty of International Relations of the Saint Petersburg University (SPbU).

Graduated from the Open University UK (second university degree) as Manager.

Career:

A career in pharmaceutical industry started in 1994, in leadership positions since 1997.

1997 - 2001 — Director CJSC «Paracels», specializing in the wholesale of pharmaceutical and medical goods.

2001 - 2006 — Director CJSC «Vertex», built the first site of the company.

2006 - 2009 — Director General and coowner of CJSC ACTIVE COMPONENT.

2009 - 2014 – President and coowner of CJSC Pervaya Pomoshch.

2009 - 2012 – Сhairman of Иoard of Вirectors CJSC «Vertex».

2009 - present - President and coowner of CJSC ACTIVE COMPONENT.

Hobby:

Alexander Semenov is fond of contemporary history, studies and monographs, plays tennis.

drago

Daniela Drago

Assistant Professor and the Director of Regulatory Affairs Programs at The George Washington University’s School of Medicine and Health Sciences

Education:

Swiss Federal Institute of Technology (ETH Zurich), Ph.D. in Chemistry.

Career:

Prior to joining academia, she worked in the pharmaceutical and medical device industries. She has held senior positions in global regulatory and medical affairs at F. Hoffman-La Roche, Vifor Pharma, Reckitt Benckiser, and Bausch & Lomb.

Her work intersects policy issues, education, and innovation. Her current research interests focus on optimizing the development of healthcare products and advancing regulatory science. She is a frequent lecturer and has published numerous articles.

Dr. Drago serves on the board of directors of the Association of Graduate Regulatory Educators (AGRE). She is the Co-chair of the Regulatory Affairs Professional Society (RAPS) DC/Baltimore Chapter and the expert advisor on regulatory competencies for The Organisation for Professionals in Regulatory Affairs (TOPRA).

zagorskiy

Andrey Zagorskiy

Director of National Immunobiological Company OJSC

Education and career:

Andrey Zagorskiy graduated from the Far Eastern State University and mastered the MBA program at the Stockholm School of Economics. He gained vast administrative experience, while taking managerial positions at large oil, energy companies and in the area of retail, having achieved impressive results everywhere, particularly, he headed Yakutgazprom OJSC (YATEC), managed the projects relating to the modernization of Zarubino Port and the Coal Terminal at the port of Eastern Fesco Group. Since 2016, he has worked as General Director of Farm Tsentr CJSC Managing Company and has been involved in the development of Sintez plant in Kurgan (it is a part of Nacimbio) and Biocom in Stavropol.

In August 2017, he has headed National Immunobiological Company OJSC.

stepkina

Elena Stepkina

Head of Implementation and Development of Good Pharmaceutical Practices and International Standards Department of the «National Center for Expertise of Medicines, Medical Devices and Medical Equipment of the Ministry of Health of the Republic of Kazakhstan»

Education:

Graduated from Almaty State Medical Institute, Pharmaceutical Faculty in 1992 cum laude. Specialty - Pharmacy. Qualification - Pharmacist, Ph. D. (Pharmacy), specialty 15.00.01 "Technology of medicines and organization of pharmaceutical business"

Career:

1992-2007: Almaty State Institute for Advanced Training of Doctors, Senior Lecturer of the Department of Pharmaceutical Management.Professional activity: Scientific and educational (extended education).

2007-2008: Institute for Health Development of the Ministry of Health of the Republic of Kazakhstan, Head of the Office for Development of the Medical Technology Assessment System.Professional activity: Scientific and educational (extended education).

2009-2015: Higher School of Public Health of the Ministry of Health and Social Development of the Republic of Kazakhstan, Head of the Academic Department "Management in Health Care and Pharmacy". Professional activity: Scientific and educational (extended education).

2015-present: Head of Implementation and Development of Good Pharmaceutical Practices and International Standards Department of the «National Center for Expertise of Medicines, Medical Devices and Medical Equipment of the Ministry of Health of the Republic of Kazakhstan». Professional activity: inspection, expert, scientific, educational.

June 04-06, 2012 Elena was a member of the working group of the Ministry of Health of the Republic of Kazakhstan on the development of the State compulsory educational standard draft of the Republic of Kazakhstan for the master's degree in the specialty "Health Management".

December 2013-2014 she was a member of the working group of the Ministry of Health of the Republic of Kazakhstan for the development of new State standards for extended education.

Elena is a member of the International coalition CoRSUM (for the safe and rational use of medicines).

2014-2015: member of the working group of the Ministry of Health and Social Development of the Republic of Kazakhstan on technical support and institutional strengthening of the National Observatory of Human Resources for Healthcare of the Republic of Kazakhstan. Also Elena participated in a workshop meeting with international WHO consultants on improving the tracking system, planning and forecasting of human resources for health.

Спикеры. День второй, 19 сентября

mezhlumyan

Armen Mezhlumyan

Winner of First Russian Interuniversity GxP Summit with international participation "Choice of the Best. Time Forward"

Education:

Pirogov Russian National Research Medical University, Pharmaceutical Faculty, 5th year student.

Professional interests:

State regulation in the sphere of medicinal products circulation;

Harmonization of Russian legislation in the sphere of medicinal products circulation with the principles of good regulatory practice (GRP);

The unified market of the Unified Energy System: issues of a unified system of state registration and recognition of registration certificates in the EAEU member countries, unified documentation of the EAEU, etc .;

Coordination and optimization of the registration dossier formation process;

Creation of forms of documents in the registration dossier that are not regulated by the current legislation;

Methods of optimization and coordination of information flows during the state registration of medicines.

Additional information:

Excellent academic performance in all disciplines (average score - 4,9);

Winner of the XII International (XXI All-Russian) Pirogov Scientific Medical Conference of Students and Young Scientists in the "Pharmacy" section (diploma of the I degree of the contest of students' reports , the topic of work: "Legal analysis of the stage of formation of a registration dossier for a medicinal product for medical use");

Winner of the 1st All-Russian inter-university GxP-summit with international participation “Choice of the Best. Time Forward” (diploma for I place);

Prize-winner of the II Inter-University Olympiad in Organic Chemistry;

Member of the educational project Pharmtech Tutor, which is held at the exhibition Pharmtech & Ingredients.

eskribano

Belen Escribano

Head of Department
Pharmaceutical Inspection and Enforcement Department
The Spanish Agency of Medicinal Products and Medical Devices (AEMPS)

Education:

University Complutense of Madrid, holds a doctorate (PhD) in Pharmacy

Career:

In 2010 she chaired the EU Council Working Party on pharmaceuticals and medical devices during the Spanish Presidency of the EU, when the falsified medicines directive was being discussed and also has participated in the GDP Drafting Group of the EMA for the update of the EU GDP guidelines. She was actively involved in the implementation of Directive 2011/62/EU at national level, including the new EU GDP guidelines. Currently she works in the implementation of the safety features regulation
and chairs the Steering Committee of WHO Member State Mechanism on substandard/spurious/falsely-labelled/falsified/ counterfeit medical products since January 2017.

loginovskaya

Olga Loginovskaya

Quality and Corporate Development Director of Flex Databases

Education:

In 1992 graduated from First Saint Petersburg State Medical University named after Pavlov, Faculty of general medicine and then clinical residency in cardiology in Research Institute of Cardiology named Almazov.

Career:

Since 1989, she has been engaged in clinical research, having started work at CRO Evidence CPR (c 2008 WCT), where for 22 years of work in various positions she gained extensive experience in this field, starting from the position of the clinical trials monitor, then the project manager of international studies.

Since 2002 - Head of Quality Assurance Department. Since 2005 - Vice President of Operations, supervised the work of the clinical, regulatory departments, the training department, translations, logistics, drug safety and a warehouse of clinical research materials. Olga spent more than 8 years as a GCP coach. Since 2009, she has taken the position of global director for training and quality management of WCT, where she was responsible for cooperating with more than 50 countries.

Since 2011, has become one of the leaders of Flex Databases, which specializes in developing software for managing clinical trials. Also currently Olga is an assistant at the Academic Department of Clinical Pharmacology and Evidence-Based Medicine at the Pavlov First St. Petersburg State Medical University.

zhuravlev

Roman Zhuravlev

Senior specialist of the drug safety department JSC R-PHARM, Ph.D

Education:

In 2005 he graduated from the medical faculty of the Peoples Friendship University of Russia, the specialty "Medicine", in 2006 graduated from the internship at the Department of Hospital Therapy, from 2006 to 2010 he studied at the postgraduate course at the Department of General and Clinical Pharmacology, in 2010 he was awarded the Ph.D. degree in the specialtie " General pharmacology, clinical pharmacology "and" Cardiology ".

Career:

Since 2009, he worked in the Scientific Center of the FSBI "Scientific Centre for Expert Evaluation of Medicinal Products" of the Ministry of Health of the Russian Federation as a researcher at the Federal Center for Monitoring the Safety of Medicines (FC MSM), and then as a senior researcher at the Center for the Examination of the Safety of Medicines (CE SM). He took part in the creation of the section "Pharmacovigilance" of the AIS Roszdravnadzor. Since August 2013 until now he has been working in the Pharmaceutical Products Safety Department of the Medical Department of R-PHARM.

romanov

Boris Romanov

Deputy Director General for Scientific Work of the “Scientific Center for Expert Evaluation of Medical Products” of the Ministry of Health of the Russian Federation

Education:

In 1992 graduated from Ryazan State Medical University named after academician I.P. Pavlov, Ph. D. (Biological Chemistry), assistant professor (Academic Department of Pharmacology with a course of pharmacotherapy).

Career:

1984 - 2001 - doctor, senior laboratory assistant, trainee teacher, graduate student, assistant professor of pharmacology with a course of pharmacotherapy at the Faculty of Postgraduate Education, curator of the cycle of professional retraining "Clinical Pharmacology", Ryazan State Medical University named after academician I.P. Pavlov (Ryazan). Polyclinic of the Ryazan Regional Clinical Cardiology Dispensary, I-st regional clinical cardiology dispensary (Ryazan).

1993 - 2011 - medical representative, promotion manager, director of hospital sales, regional director, medical director in international and domestic pharmaceutical companies.

2002 - 2004 - Assistant Professor of the Academic Department of Biochemistry of the Medical Faculty of the RUDN (Moscow).

2002 - 2011 – Senior research scientist of Scientific-Research Center scientific group; Assistant Professor of Farmacology Department; Senior Specialist of Department for pre-clinical and clinical trials of medicines organization; Professor of Pharmacology Department, Head of Educational Board of Pharmacology Department, Authorized Person for the quality of educational and scientific work of the Pharmaceutical faculty of the First Moscow State Medical University named after I.M. Sechenov (Moscow).

Since 2011 - present - Deputy Director General for Scientific Work of the “Scientific Center for Expert Evaluation of Medical Products” of the Ministry of Health of the Russian Federation.

Author of university and post-university federal educational programs: «GXP – system of Good Practices: GEP, GMP, GLP, GCP, GDP, GPP, GVP» (2006), «Product management» (2006), «Advance Management» (2006), «Ensuring and monitoring the quality of medicines production – GMP» (2006), «Clinical trials of medicines» (2007).

french

Yvonne French

Divisional Vice President Quality Assurance at Abbott Products Operations AG

Education:

Obtained a Bachelor’s degree in Science from the University of Dublin, Ireland.

A Master’s degree in Pharmaceutical Manufacturing and Technology from Trinity College, Dublin, Ireland and a Diploma in Quality Management.

Professional experience:

Joined Abbott in 1991 as a QA Laboratory Supervisor/Microbiologist at the Sligo, Ireland device facility.

Held several leadership roles with over 25 years’ experience gained in both the Medical Device and Pharmaceutical Divisions.

Have experience in leading start-ups from Greenfield through validation to fully operational plants including FDA/EMEA approvals.

Held the role as Divisional Vice President, Quality Assurance and Compliance, Abbott Medical Optics, based in California USA, from June 2013 – March 2017.

Assumed current role as Divisional Vice President Quality Assurance at Abbott Products Operations AG, based in Allschwil, Switzerland.

chang

Andrew Chang

Vice President, Quality and Regulatory Compliance Management, Novo Nordinsk A/S, earlier - Deputy Director of FDA on Policy and Regulations (USA)

Dr. Andrew Chang has more than twenty years of experience in the development, regulation and quality of biologics and pharmaceuticals. At his current capacity as a Vice President, Quality and Regulatory Compliance, Product Supply Quality Compliance Management, Novo Nordisk A/S, he is responsible for providing strategic advice and solutions for quality and regulatory related issues and expert support to inspection preparation. Since 2013, Andrew has represented Novo Nordisk at several work groups in industry trade organizations, e.g., PhRMA, EFPIA, BIO and RDPAC to advocate patient and industry’s interests by developing position papers and participating liaison meetings with the regulatory authorities. He is also a member of PhRMA’s ICH Work Group, and representing PhRMA as an expert to ICH Q12 Expert Working Group for developing guideline on Pharmaceutical Products Lifecycle Management.

Prior to Novo Nordisk, Andrew served more than eleven years at US FDA, most recently as an Associate Director for Policy and Regulation, Acting Deputy Director and Senior Regulatory Scientist in the Division of Hematology, Center for Biologics Evaluation and Research (CBER). During his tenure, Andrew received numerus high level FDA awards for his exceptional and outstanding performance on regulatory review and management, GMP inspection, and policy development. These include, but are not limited to FDA Commissioner's Special Citation for successfully completing FDA’s initiative on product quality regulation and CBER’s Public Health Achievement Award for outstanding regulatory review performance that resulted in averting a crisis in product availability. In 2002, the FDA recognized Andrew as the FDA regulatory expert in the regulation of new and novel recombinant products as well as naturally-derived biological products.

Andrew’s formal scientific training includes post-doctor in immunology from the National Institutes of Health, Ph.D. in Biochemistry from the State University of New York, and B.S. in Pharmaceutical Chemistry from the China Pharmaceutical University. He has published numerus peer reviewed scientific papers in JAMA, J.Exp.Med., Blood, J.Immunol., Dev. Immunol. Thromb Haemost., Haemophilia, Pharmaceutical Engineering etc., and has been a frequent speaker at national and international conferences.

garsiya

Marcelo Sidi Garcia

Specialist in Brazilian Health Regulatory Agency

Education:

Graduate in Marketing: Marketing
Academic background: Pharmacy
Health Education - UNB
Sanitary Surveillance - Fiocruz.

Career:

Works in Medicine and API inspection.

Experience in Pharmaceutical Industry for 10 years.

Worked on the marketing authorization area.

Participation in the activities of Anvisa's Management Improvement / Strategic Planning Program.

gaydash

Kyrill Gaydash

Acting General Director of the Federal State Unitary Enterprise "NPO" MICROGEN "of the Ministry of Health of Russia

Education:

In 1995 he graduated from the State Academy of Management named after S. Ordzhonikidze, majoring in Information Systems in Management.

Career:

Worked in JSC SAVINGS BANK of the Russian Federation (PAO), and also held senior positions in the Group of Companies "Agency for the Restructuring of Credit Organizations" and OJSC "BANK VTB".

Since 2008, he was the Director for Economics and Finance of the State Corporation ROSTEC, where he was involved in the formation of the economic, financial and budgetary policies of the Corporation, the formation and control of the implementation of the budgets of the Corporation's organizations, attracting budgetary and extrabudgetary funds and programs to increase the value of assets, other issues of the financial and economic activities of the Corporation.

Since 2015 he is General Director of the Federal State Unitary Enterprise "NPO" MICROGEN "of the Ministry of Health of Russia.

Awards:

ssigned the title of "Honored Economist of the Russian Federation".

valiev

Artur Valiev

General Director of LLC SAN PHARMA Russia, Ph.D. (Medicine)

Education:

Kazakh scientific research dermatovenerologic institute. Clinical Residency - Urology Research Center. Academician B.U. Jarbusynova (urology and nephrology). The general practice doctor Almaty State Medical Institute.

Career:

Artur Valiev has 17 years of experience in managing multifunctional pharmaceutical organizations in Russia and the CIS, which are part of multinational global corporate structures, in the sphere of import and export, trade, management, regulation, regulatory management and supervision, and research functions.
Development of companies' business through mergers and acquisitions of companies and / or individual parts of the business. Allocation of corporate structures from controlling company. Design, construction and modernization of production and control-analytical pharmaceutical production, and laboratories.
Since April 2016 – till now the General Director of San Pharma Russia.

November 2015 - February 2016, Managing Director of the VACCINA sub-holding. National Immunobiological Company (a subdivision of Rostekh State Corporation).

March 2015 - November 2015 - President of AstraZeneca Kazakhstan, AstraZeneca Eurasia.

October 2010 - December 2014 - Regional Director for Russia and CIS ZOETIS. ZOETIS Inc. USA (former Pfizer Animal Health). General Director of OOO ZOETIS, Russia. Acting General Director of LLC ZOETIS Ukraine (November 2012 - July 2013).

December 2007 - September 2010 Director of Marketing & Sales Janssen-Cilag Russia, Member of the Board of Janssen-Cilag of Russia. Janssen-Cilag, Pharmaceutical Division Johnson & Johnson, USA.

May 2000-December 2007 Director General of Janssen Cilag in Kazakhstan and Central Asia.

ahantiev

Andrey Akhantiev

Director for Economic Security, Group of companies "GEROFARM"

Education:

He was born in 1960 in Novosibirsk. He graduated from the Pacific Higher Naval School named after S.O. Makarov in Vladivostok. During the military and civil service he held various positions of senior management. He received additional education under the programs of retraining of economic and business orientation at the Far Eastern Federal University.

Career:

After dismissal from the civil service he worked in the line of economic security in business structures.

Is working in the GC "GEROFARM" since 2008. He passed additional training in the sphere of economic and information security of business, state contracts system.

He is an expert and a constant participant of the largest thematic conferences, round tables devoted to the issues of legislative regulation in the pharmaceutical industry, actively participates in the work of expert groups and meetings with regulators.

glushkov

Ivan Glushkov

Director of the Department of External Relations of OJSC NIZHPHARM (STADA Group of Companies)

Education:

Lomonosov Moscow State University, Chemical Faculty and Plekhanov Russian University of Economics, Economic Faculty.

Career:

For a long time he has worked as a manager in the company IBS (Information Business Systems), where he was engaged in management consulting. He was the financial director of the Moscow Cardboard and Polygraphic combine of complementary industrial plants, and for four years he had been working as a Partner of the auditing and consulting company Baker Tilly Rusaudit.

Since 2004, Ivan Glushkov has been with STADA, where he is a Director of the External Relations Department. Mr. Glushkov also coordinates the work of regional offices in the Baltic countries, Ukraine, and Central Asia.

In 2015, Ivan Anatolyevich was elected as a Chairman of the Board of the Kaluga Pharmaceutical Cluster. Ivan Glushkov is a member of the Committee on Entrepreneurship in the Health and Medical Industry of the Chamber of Commerce and Industry of the Russian Federation, expert councils of the Commission of the Customs Union and the Federal Antimonopoly Service, the project group of the Ministry of Industry and Trade of the Russian Federation, the General Industry Expert Group on GMP SPFO, which works to consolidate the views of recognized Russian and international experts in the field of implementing the international principles of GMP and to assist the Ministry of Industry and Trade of the Russian Federation.

titova

Lily Titova

Executive Director of the Union of Professional Pharmaceutical Organizations (SPFO)

Education:

Graduated from the Moscow Medical Academy named after I.M. Sechenov, specialty "Pharmacist".

Career:

She worked in the Ministry of Health of the RSFSR, the USSR, Russia, including as Deputy head of the Department for the organization of the provision of medicines and medical equipment of the Ministry of Health of Russia (1999-2000).

1994-1998 - Marketing Director of CJSC Bryntsalov A.

2000-2005 - Deputy Director for Pharmaceutical Activities, State Unitary Organization "Zheldorfarmatsia of Russian Railroads".

In 2005 was elected General Director of the ARPP (Association of Russian Pharmaceutical Manufacturers), where in 2007 she moved to the position of Deputy Assistant to the Head of Roszdravnadzor.

From the end of 2008, she was the General Director of LLC "Pharmaceutical Industry" (as part of ARPF).

October 14, 2014 was elected Executive Director of the SPFO.

tkachenko

Maxim Tkachenko

Member of the Board of Directors of PJSC "Farmimex", Director of Procurement

Education:

In 1994 graduated from Minsk Higher Military Engineering School with honours. During the period of military service he was scientific employee of the Research Institute of the Ministry of Defense of the Russian Federation. Mr. Tkachenko received supplementary education in The Open University (UK) on the marketing and business management programs.

Career:

Maxim Tkachenko has been working in the pharmaceutical market more than 20 year. He started his activity in the pharmaceutical business in 1997 working in distribution company CV "Protek". He was responsible for company branches inventory supplement, management and development of assortment. Maxim Tkachenko participated in ERP-system implementation, development and optimization of distribution business processes.

From 2009 he has been working in PAO «FARMIMEX». Mr. Tkachenko is a member of Board of Directors, he is responsible for procurement management and is in charge of Procurement Department, and also he is a part-time compliance officer. Mr. Tkachenko participated in the updated ERP-system SAP/R3 implementation. In accordance with company development strategy Mr. Tkachenko is actively searching for new and innovative foreign medicines and their launch into the Russian pharmaceutical market.

krylov

Igor Krylov

Managing Director of Marathon Pharma sub-holding

Education and career:

Having graduated from the S.M. Kirov Military Medical Academy in 1987, a military physician Igor Krylov served in the Russian army until 1994.

In 1994-2002, he worked at the Russian representative office of the international pharmaceutical company Eli Lilly and Company, where he was responsible for marketing of endocrine preparations, and thereafter at Aventis, where he ensured the launch of the company’s insulin production.

In 2008-2014, he headed Farmstandard, having turned it into the leader of industry, and then, as First Vice President, developed Medsi clinic network.

In 2017, he joined the Marathon Group team as Managing Director of Marathon Pharma sub-holding.

Спикеры. День третий, 20 сентября

muhina

Sofia Mukhina

Manager for quality assurance of LLC “ISAI RUSSIA” Sofia Mukhina

Education:

Graduated from Moscow State University of Fine Chemical Technology. M.V. Lomonosov Moscow State University, degree in biotechnology and pharmaceutical technology in 2012.

Career:

From 2012 to the present time she has worked in Pharmapark LLC, Novartis Pharma LLC, Astellas JSC, Asai LLC (current place of work). In the course of her work she was engaged in the development and creation of new liquid dosage forms, the improvement of the quality management system, the returns and claims of consumers, the investigation of complaints and deviations, the technical support of warehouse processes, the interaction with regulatory bodies in the field of medicinal products, the training of employees on quality, contractual organizations, service providers in accordance with the requirements of GMP and GDP, conducting supplier audits and self-inspections, document management and quality agreements, participation and communication in the future GMP inspections carried out by the health authorities (Russia and Ukraine) and others.

gumi

Stephane Gumy

General Manager PMS Process Management System and Trainer for Educational Pharma Programs at ARIAQ (Switzerland)

Career:

More than 20 years in the pharmaceutical, biopharmaceutical and medical industry in international companies (Baxter, Johnson & Johnson), as well as in small and medium companies as a leading specialist in Production, Quality Assurance and Quality Control departments, Process development.

Experience in conducting inspections with the FDA, ANVISA, WHO, Swissmedic and other national and international agencies.

Since 2007, an independent consultant and founder of the consulting company PMS Process Management System.

Since 2013, the Contract Authorized Person.

nikitina

Irina Nikitina

Candidate of Economic Sciences, Candidate of Pharmaceutical Sciences, Director of Quality Department, Group of companies «GEROPHARM»

Education:

In 1997 Irina Nikitina graduated with honors from Saint Petersburg State Chemical Pharmaceutical Academy (SPCPA) with a degree in Pharmacy.

In 2001, on the basis of SPCPA, she completed her postgraduate studies and defended her thesis for a master's degree in "Medicine technology and organization of pharmaceutical business".

In 2006 she graduated with honors from St. Petersburg University of Management and Economics, Faculty of management, specialization "Anti-crisis management". In 2015 she defended her thesis for a master's degree in «Economics and National Economy Management (Innovation Management)».

Career:

Since 2010, she has been a freelance expert in FGU «Analytical Center for the Government of the Russian Federation». Irina Nikitina participated in the projects examination of the Government of the Russian Federation and the Commission under the President of the Russian Federation on the modernization and technological development of the Russian economy in the direction "Medical equipment and pharmaceuticals".

In 2013, on the basis of IMBP RUDN (a training program in conjunction with ANO «National Institute of Innovation», LLC «Biological Safety and Protection» and ARFP) successfully mastered a course of professional retraining in the specialization "Management of technological and economic risks."

Professional activity for more than 15 years has been directly related to working in the leading positions in the fields of regulatory relations, drugs research and development, quality control and quality assurance in large Russian manufacturing pharmaceutical companies. Since February 2014 Irina Nikitina had been working as Deputy director of ZAO "Farm-Holding" for pharmaceutical development. Since July 2016 she has been as Director of the Quality department of the Group of companies "GEROPHARM".

borisov

Konstantin Borisov

Founder, CEO Support Partners

Education:

2015 - Business School Skolkovo.

2009- MBA, Academy of National Economy under the Government of the Russian Federation.

2002 - Moscow Pedagogical State University. Teacher of Russian as a foreign language, literature and foreign languages (English and German), majoring in Philology.

Career:

Since 2009-Founder and CEO of SUPPORT PARTNERS Executive Search, the leading Managers search and hunting company. Constantine also owns a rental business in the field of real estate.

SUPPORT PARTNERS cooperates with the largest Russian and foreign companies in the field of industry and the consumer goods industry, as well as with the main private equity funds. Among the clients of SUPPORT PARTNERS are such companies as Rusagro, Severstal, Tatneft, Power Machines, Rosatom, Baring Vostok, Capital Partners, Millhouse and others.

Konstantin regularly speaks to the audiences of business owners and business leaders at business conferences and round tables.

From 2000 to 2008 - from a consultant to the CEO of a number of subsidiaries of the "Anchor" Holding, he was repeatedly recognized as the best employee of the year, he was engaged in launching new business lines.

Awards:

Laureate of the rating "Top-1000 Managers of Russia" according to the Kommersant Publishing House.

Member of the General Council "Business Russia".

He is a member of TOP-10 Russian General Directors in the Professional Services segment according to Kommersant Publishing House version in 2016.

plesovskih

Anna Plesovskikh

Head of Department of External Communications of FSI “SID & GP”

Education:

Graduated from Novosibirsk State Technical University a degree in PR in 2006, during studies worked in various publications as a correspondent.

Career:

In 2006, she got a job at the "Novosibirsk city website", engaged in development and promotion. 2008, moved to Novosibirsk HR services holding "ANCOR", where she held the position of Marketing Coordinator (2008), marketing Manager for Siberia and the Far East (2010), Deputy Head of Marketing in Russia (2011), Deputy Head of Marketing in Russia with relocation to Moscow (2012) and Marketing Manager (2015).

2017, became a Deputy Head of Department of External Communications of FSI “SID & GP” with the subsequent rise to the position of Head of the Department.

orlov

Vladimir Orlov 

Deputy Head of Educational Center of the FSI “SID & GP”

Education:

Saint-Petersburg State Chemical-Pharmaceutical Academy.

Additional trainings in a field GMP/GDP-inspection/audit; GMP-Inspector.

Career:

His career was started at the enterprise on the manufacture of active pharmaceutical ingredients. Since 2008 to 2013 worked at STATE RESEARCH INSTITUTE OF HIGHLY PURE BIOPHARMACEUTICALS (Saint Petersburg) as Validation Engineer. In 2013-2014 worked in the city of Kaluga during the launch phase of asite to produce insulin "Novo Nordisk", where he was engaged in manufacturing of aseptic and sterile production. Since 2014 began work in the newly created Department of inspection of the FSI "SID and GP" as the leading expert-auditor. November 2016 was to combine the primary activity with the position of the Head of the laboratory of GMP of the Education Centre of the FSI "SID and GP".

vazmina

Tatiana Viazmina

Quality Director JSC R-PHARM

Education:

Graduated from University of Chemical Technology of Russia named after Dmitry Mendeleev, qualified as Technical engineer.

Career:

Since 2003, he has held various management positions in the quality field of a number of large high-tech innovative pharmaceutical companies. Since April 2015, he has been managing the Quality Department of the R-Pharm Group of Companies.

tarasov

Tarasov Vadim

Director of the Institute of Pharmacy and Translational Medicine of the Federal State Autonomous Educational Institution of Higher Education “The First Moscow State Medical University named after I.M. Sechenov” of the Ministry of Health of the Russian Federation

Education:

2009 - Moscow Medical Academy named after I.M. Sechenov, Moscow, Pharmaceutical Faculty, Pharmacy.

2012 - First Moscow State Medical University named after I.M. Sechenov of the Ministry of Health and Social Development of Russia, Moscow, Postgraduate.

Карьера:

Since 2006, he is an employee of the First Moscow State Medical University named after I.M. Sechenov of the Ministry of Health of the Russian Federation.

Scientific degree, academic status:

Ph.D. Pharmaceutical Sciences. Theme of dissertational researches: "Development and application of polymeric delivery systems for neurotropic drugs" on specialty 14.04.01 - Technology of medicines obtaining. 

pyatigorskaya

Natalya Pyatigorskaya

Deputy Director for Research of the Institute of Pharmacy and Translational Medicine, Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenovsky University)

Head of the Department of Industrial Pharmacy

Member of the Council for Professional Qualifications in Pharmacy

Education:

1988 - Moscow Institute of Fine Chemical Technology of M.V. Lomonosov. Specialty - technology of basic organic and petrochemical synthesis.

2001 - Moscow Medical Academy of I.M. Sechenov. Specialty - pharmacy.

2011 - Doctor of Pharmaceutical Sciences.

2014 - Professional retraining in the program "Teacher of higher education".

2015 – Professor.

Career:

1999-2001 - deputy director for scientific and production issues, OOO «Bivitech».

2001-2005 - deputy director for scientific and technological work of state unitary enterprise "GNII Vitamins".

2005-2007 - head of the laboratory of drug technology in research institute of pharmacy, First Moscow State Medical University I.M. Sechenov.

2005-2012 - assistant professor of the department of organization of production and distribution of medicines, First Moscow State Medical University I.M. Sechenov.

2012 - 2017 - professor of the department of industrial pharmacy, First Moscow State Medical University I.M. Sechenov.

2007 - present - deputy director for scientific work of the Institute of pharmacy and translational medicine. First Moscow State Medical University I.M. Sechenov.

2017-present. – head of department of industrial pharmacy, First Moscow State Medical University I.M. Sechenov.

Achievments:

The author of exemplary educational programs for further vocational education in industrial pharmacy, approved by the Order of the Ministry of Health of Russia from 22 January 2014 No. 37n.

The author of the new training program Industrial Pharmacy (Order of the Ministry of Education and Science of Russia from 01.12.2016 № 1508).

Author of the Federal State Education Standard in the field of education 33.04.01 Industrial pharmacy (master's level), approved by the Order of the Ministry of Education and Science of the Russian Federation from July 26, 2012 № 705.

Author of 5 professional standards for specialists in industrial pharmacy.

Author of new professions for specialists in industrial pharmacy.

News