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20th - 22nd April 2021
★ 100% virtual conference ★Presented in Central European Time (CET)

Edelgard Rehak
Consultant at Edelgard Rehak Consulting

Profile

Dr. Edelgard Rehak is an advanced Regulatory Affairs professional with more than 20 years hands-on experience in different areas of drug development, Regulatory Affairs, and quality assurance of pharmaceutical products, biotech, and medical devices in Europe, Russia, and CIS countries (former Soviet Union countries).

She has been working around 8 years locally in Moscow and Kyiv (capital of Ukraine) for Pharma companies such as Novartis and Sanofi and held executive positions in Regulatory affairs.

Prior to that, she has been working in product development (generics and biosimilars) and clinical research at Sandoz/HEXAL, Germany.

Now Dr. Rehak lives in Berlin, runs her consulting company, and offers expert solutions in Regulatory Affairs, GMP Audits, and Due Diligence for Russian, Eurasian Economic Union, and CIS market.

Agenda Sessions

  • Guidance on Launching Products in Russia/ EAEU and CIS Countries

    13:20