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MedTech Summit
Hybrid Event, 20 - 24 June 2022
In-Person: Clayton Hotel Burlington Road, Dublin, IrelandDigital Experience: One track will be live-streamed each day in BST time zone, with on-demand recording access for all other tracks made available from the afternoon of the following day. Learn more on the Digital Experience page.

Arkan Zwick
Corporate Regulatory Affairs Director at Croma Pharma

Profile

After his graduation in European law Dr. Arkan Zwick spent seven years in Public European affairs at the City of Vienna Business Agency and the European Commission in Brussels as Head of unit European Information Centre Network (EIC) and project manager for EU regional development funds. Fifteen years ago he joined the Medical Device & Pharma Industry as Corporate Director for Regulatory Affairs for ophthalmology, orthopedic and aesthetic dermatology products. He is responsible for regulatory advocacy for drug, medical devices and combinations products compliance as well as in house legal advice for contract management, M&A and due diligence. His activities cover global regulatory interaction with notified bodies, competent authorities, medicinal agencies and European Commission and global regulatory market access in the EU, Americas and Asia-Pacific including Health Canada, FDA, ANVISA, NMPA and TGA. Arkan is lecturer and Trainer at the University of Applied Sciences in Vienna and speaker on life cycle conferences and seminars.

Agenda Sessions

  • Annex XVI – Common Specifications

    09:40
  • Annex XVI – Common Specifications

    15:00