March 6, 2024
3 pm (Chinese time)
45 minutes
FREE Webinar
俄罗斯的临床试验和药品注册
Clinical Trials and Drug Registration in Russia
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 Russian market grows, more questions on regulatory and procedural aspects of conducting clinical trials, registering new drugs and passing GMP inspections keep emerging. 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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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
GMP inspection requirements
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
Have a question or request? We’re here to help!
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Organiser
info@oct-rus.ru