Natasha Bankowski
Natasha holds a BSc in Medicinal Chemistry from Trinity College Dublin and has completed additional Higher Diploma modules in Pharmaceutical Production. With over 17 years of experience in the pharmaceutical and medical device/IVD industries — 12 of which have been in senior leadership roles — she brings extensive expertise across global regulatory affairs, pharmacovigilance, quality assurance, operations, clinical and medical information, R&D and project management.
Natasha is an active member of the TOPRA MedTech Working Party and is a frequently speaker at industry conferences. She was recently named among the Top 100 MedTech Leading Voices on LinkedIn. Natasha lectures and assesses part-time on BSc and MSc Global Regulatory Affairs courses at universities in Ireland and the UK.
JournalIVD5: Navigating conformity assessment for IVDs – Challenges and opportunities
This is a report of the HM5/MD1/IVD1 session that took place at this year’s Symposium.
JournalHM3: Applying Artificial Intelligence in real life
This is a report of the HM3 session that took place at this year’s Symposium.
