Jan 27: Visiting from Glasgow- Europe MedTech Regulatory Workshop

Europe MedTech Regulatory Workshop, with Edward Staunton. Tuesday, January 27th, 9-11am, Herzog Towers, 6 Sadeh, Tel Aviv.

Visiting from Glasgow, Edward Staunton's session is for Founders who don’t have time for guesswork. Cut through the noise of EU MDR, IVDR, notified bodies, and market entry hurdles. This workshop distills the regulatory maze into the precise steps MedTech teams need to move from prototype to approval. Venue is Herzog Towers, 6 Sadeh, TLV.

Key Sections:
• Breakdown of the EU regulatory landscape
• Practical guidance on classification, documentation, timelines and BUDGET
• Best practices for navigating compliance

This hands-on workshop will help you overcome regulatory hurdles and make Europe a launchpad, instead of a bottleneck.

Title: Europe MedTech Regulatory Workshop, with Edward Staunton
Keynote: Edward Staunton, Director, Regulatory Affairs & Quality, Clinigen. He will be joined by Fredrik
Time: 9-11am (content: 9:30-10:30am)
Venue: Herzog Towers, 6 Sadeh, Tel Aviv
MC: Goel Jasper, FINN Partners
Agenda:
9:00-9:30 Registration and networking
9:30-9:35 Welcome Remarks, Goel Jasper
9:35-9:45 Introduction to Clinigen, Mel Wallace, VP, Clinical Supplies Management
9:45-10:35 EU MedTech Regulatory Workshop, led by Edward Staunton
10:35-10:45 EU MedTech Go-to-Market insights, Frederik Johanssen

See you on Tuesday, January 27th, 9-11am at Herzog Towers, 6 Sadeh, TLV, for Europe MedTech Regulatory Workshop, with Edward Staunton.