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

Natasha Bankowski
Director of Regulatory Affairs and Quality Assurance at Beyond Air


Natasha recently joined Beyond Air Inc as Director of Regulatory Affairs and Quality Assurance and is based in Dublin, Ireland.

Natasha graduated with a BS in Medicinal Chemistry from Trinity College, Dublin and completed further Higher Diploma modules in pharmaceutical production. Natasha has a broad range of experience working in both the Pharmaceutical and Medical Device Industry for over 15 years.

She has worked across multiple areas including Quality Management, Regulatory Affairs, Medical Affairs, Pharmacovigilance and R&D. She has managed the Global Regulatory Affairs, Quality Assurance, Pharmacovigilance and Clinical/Medical Affairs departments for both medicines and medical devices, working for companies such as the HPRA, LEO Pharma, Omega Pharma, Abbotts and Kora Healthcare and Phoenix Healthcare.

She has been successful in directing the global strategy, gaining approval, and building the global footpath with registrations in over 150 countries in a wide range of therapeutic areas.

She was ultimately responsible for implementation of the MDR, UDI, Serialisation and Brexit in her last few companies.

Natasha has been lecturing on the Global Regulatory markets and Post-Market Surveillance modules for Irish MedTech Association skillnet courses in Ireland since 2017 delivering lectures via University of Limerick and GMIT, Ireland.

Natasha is a member of the TOPRA working party for medical devices where she organises the Annual Symposium and one of the members responsible for the agenda and all speakers. She recently chaired a Global MedTech conference for Informa Life Sciences.

Agenda Sessions

  • Industry Panel: Adhering to all European Requirements

  • Industry Panel: Interpreting the MDR