December 16, 2024
3 pm (Chinese time)
45 minutes
FREE Webinar
Pharmaceutical cooperation between Russian and Chinese companies have been gaining strength over the past several years. Numerous partnerships prove this case. Nonetheless, as the interest towards the Russian market grows, more questions arise on regulatory and procedural aspects of conducting clinical trials and registering new drugs. To that end, the experts from OCT, a leading Russian and Eastern European CRO, will shed light on these questions and cover them during this webinar.
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在俄罗斯和欧亚经济联盟中进行临床试验和药品注册
Clinical Trials and Drug Registration in Russia and EAEU
Registration form
fill out in English
You will learn:
How to register a drug in Russia
Local regulatory framework
Registration strategies for biologics, chemical drugs and herbal medicines
How to conduct clinical trials in Russia
Keynote Speakers
Sarizha Magomedova
Head of Drug Registration
Eugenia Radkova
Head of MedSci Consulting and Excellence
Irina Petrova
Head of Clinical Operations
Who will benefit:
Head of clinical operations
Medical officers
С-Suite pharmaceutical
Scientific officers
R&D
Biostatisticians and medical writers
Clinical operations
Market access managers
Regulatory managers
Clinical trial management
Registration form
Please, fill out the form in English
