The only international event dedicated to discussing regulatory, ethical and operational aspects of running clinical trials in Russia

1 - 2 December 2020

Marriott Grand Hotel, Moscow, Russia

Confirmed speakers:

Dmitry Schekin, Deputy Head of the Division for Coordination of Work on Pharmaceutical Drugs and Medical Devices Circulation, Department for Technical Regulation and Accreditation, Eurasian Economic Commission
Dmitry Schekin

Deputy Head of the Division for Coordination of Work on Pharmaceutical Drugs and Medical Devices Circulation, Department for Technical Regulation and Accreditation

Eurasian Economic Commission

Dmitry Rozhdestvensky, Head, Division for Coordination of Common Market for Drugs and Medical Devices Formation, Eurasian Economic Commission
Dmitry Rozhdestvensky

Head, Division for Coordination of Common Market for Drugs and Medical Devices Formation

Eurasian Economic Commission

Oleg Talibov, Associate Professor of the Department of Therapy, Clinical Pharmacology and Ambulance, Moscow State Medical University
Oleg Talibov

Associate Professor of the Department of Therapy, Clinical Pharmacology and Ambulance

Moscow State Medical University

Artem Poltoratskiy, Head of the Department for Pre-Clinical and Clinical Trials, National Medical Research Centre of Oncology Named after N.N.Petrov
Artem Poltoratskiy

Head of the Department for Pre-Clinical and Clinical Trials

National Medical Research Centre of Oncology Named after N.N.Petrov

Sergey Dubrovin, Site Relationship Partner (Director), Russia and Belarus, Pfizer
Sergey Dubrovin

Site Relationship Partner (Director), Russia and Belarus

Pfizer

Vladimir Bulatov, Chief Scientific Officer, Novartis Pharma, Russia
Vladimir Bulatov

Chief Scientific Officer

Novartis Pharma, Russia

Tatiana Goldina, Data Generation & Scientific Communication Lead, Medical Affairs, Sanofi
Tatiana Goldina

Data Generation & Scientific Communication Lead, Medical Affairs

Sanofi

Alina Mustafina, Medical devices department lector, RMANPO
Alina Mustafina

Medical devices department lector

RMANPO

Maria Leer, Head of Medical Projects Group, Takeda
Maria Leer

Head of Medical Projects Group

Takeda

Julia Trakhtenberg, Medical director, IPHARMA
Julia Trakhtenberg

Medical director

IPHARMA

Mikhail Samsonov, Chief Medical Officer, R-Pharm
Mikhail Samsonov

Chief Medical Officer

R-Pharm

Vladimir Vasilyev, Compliance Process, Training & Systems Manager, PDG Country Clinical Operations, CEETRISMEA, F.Hoffmann-La Roche Ltd.
Vladimir Vasilyev

Compliance Process, Training & Systems Manager, PDG Country Clinical Operations, CEETRISMEA

F.Hoffmann-La Roche Ltd.

Yuri Zaretskiy, Managing Director, ZM Company Inc
Yuri Zaretskiy

Managing Director

ZM Company Inc

Victoria Kosmacheva, Clinical Research Manager, GlaxoSmithKline
Victoria Kosmacheva

Clinical Research Manager

GlaxoSmithKline

Olga Melnik, Head of Clinical Operations, Novartis Pharma
Olga Melnik

Head of Clinical Operations

Novartis Pharma

Almira Galeeva, Director of Clinical Research & Medical Affairs, AIPM Russia
Almira Galeeva

Director of Clinical Research & Medical Affairs

AIPM Russia

Yunona Khomitskaya, Medical Director, Servier
Yunona Khomitskaya

Medical Director

Servier

Francis Crawley, Executive Director, Good Clinical Practice Alliance - Europe (GCPA), Belgium
Francis Crawley

Executive Director

Good Clinical Practice Alliance - Europe (GCPA), Belgium

Ludmila Grivcova, Head of laboratory medicine, head of clinical immunology laboratory, FSBI NMRRC of the Ministry of Health of the Russian Federation
Ludmila Grivcova

Head of laboratory medicine, head of clinical immunology laboratory

FSBI NMRRC of the Ministry of Health of the Russian Federation

Natalya Falaleeva, Head of department, FSBI NMRRC of the Ministry of Health of the Russian Federation
Natalya Falaleeva

Head of department

FSBI NMRRC of the Ministry of Health of the Russian Federation

Olga Vostrikova, Chairman, INTERNATIONAL UNION FOR PATIENT ASSISTANCE AND SUPPORT
Olga Vostrikova

Chairman

INTERNATIONAL UNION FOR PATIENT ASSISTANCE AND SUPPORT

KEY TOPICS & FEATURES IN 2020:

o   The current status of the clinical trials market: what are the latest trends in Russia and globally?

o   Clinical trials during the Covid-19 pandemic: practical experiences, challenges and solutions found

o   Clinical trials in the Eurasian Union - registration practices and common rules in action

o   Acceleration of digitalisation in clinical trials: AI, remote monitoring, electronic registers, access to data and data safety

o   RWE - globally and in Russia: RWE as a key tool for the federal project “Digital technologies”

o   Live Interviews with sponsors and research & investigators centres

Why to attend the Clinical Trials in Russia Forum in 2020?

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Insights from 40+ experts: regulators, representatives of international and Russian pharmaceutical producers, CROs and investigators

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2-day information-rich programme that includes insightful presentations from leading sector players, interactive debates and round tables

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Unrivalled networking opportunities with 150+ attendees from such companies as AstraZeneca, Pfizer, Novartis, Bayer, Biocad, R-Pharm and many more

FEEDBACK FROM ATTENDEES

Unique opportunity for all the clinical trials sector players to meet and discuss the most burning issues.

Tatiana Minakova,

Associate Director, Clinical Monitoring, Syneos Health

The forum brings together representatives of all stakeholder groups involved in clinical trials – sponsors, CROs, regulators and investigators for a constructive dialogue aimed at improving all future processes.

Julia Semenova,

Pharma Development Unit Head, Novartis Russia

Very good overview of a large number of clinical trial topics and the specifics of the Russian market.

Henryette Schatt,

JDirector eCOA Business Development, ERT (Switzerland)

Very interesting insight into the latest developments in the Russian market.

Stefanie Rau,

Clinical Trials and Pharmacovigilance Manager Europe, MUCOS Pharma (Germany)


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