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MedTech Summit

£500 SAVINGS EXPIRE IN:

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10 - 14 June 2024
DoubleTree by Hilton Brussels CityBrussels, Belgium (Hybrid Event)

Nataliya Deych
Vice President Regulatory Affairs EMEA, Latam, Canada at Edwards Lifesciences
Speaker

Profile

Qualified to a master’s degree in biotechnology, based in Geneva-Lausanne area in Switzerland and working as a Vice President Regulatory Affairs EMEACLA (Europe, Middle East, Africa, Latin America, and Canada). In Nataliya’s current role she is directing and influencing regulatory strategies and guide the company through multiple regulatory changes and dynamics, including investment into capabilities and competitive edge also in the area of digital health. Nataliya also has a special focus on regulatory and clinical pathways to accelerate marketing authorization and patient access, that also includes the risk benefit approach in clinical evidence and Real World Evidence especially for therapies that address unmet medical needs. Prior to joining Edwards she was a Sr. Director Regulatory Affairs EMEA at Medtronic, headed up Regulatory Affairs at Colgate-Palmolive Europe Sarl. in Basel, Switzerland. Nataliya previously held the management positions in Research and Development, Manufacturing Process Management and Quality Assurance at Unilever company, and worked as an independent consultant to the cosmetic industry and for alternative toxicological methods.

Agenda Sessions

  • Shared Experiences: Navigating Clinical Evaluation and Performance Evaluation Consultation Procedures (CECP/PECP)

    11:10