Postponed (due to EU travel restrictions): EU MedTech Regulatory & GTM

POSTPONED due to EU travel advisory. The speakers WILL come to Israel but are forced to delay this trip due to the EU travel advisory.

Three experts, coming from Glasgow, Stockholm and London: Europe MedTech Regulatory & Go-To-Market Workshop, with Edward Staunton, Fredrik Johansson and Mel Wallace..

Cut through the noise of EU MDR, IVDR, and market access challenges. Experts with decades of experience share their practical regulatory and GTM best practices. Venue is Herzog Towers, 6 Sadeh, TLV.

Key Sections:
• Breakdown of the EU regulatory landscape, including compliance
• Guidance on classification, documentation, timelines and BUDGET
• Hospital pilot structures that prove cost savings in real workflows
• Economic cases tailored to payer and hospital incentives

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

Title: Europe MedTech Regulatory & GTM Workshop, with Edward Staunton, Fredrik Johansson and Mel Wallace
Speakers: Edward Staunton, Director, Regulatory Affairs & Quality, Clinigen.
Fredrik Johansson, Director, Business Development, Commercial Strategy, Clinigen
Mel Wallace, Vice President, Clinical Supplies Management, Clinigen
Time: 9-11am (9:30 start)
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
9:35-9:40 mHealth Israel Introductory Remarks
9:40-9:50 Introduction to Clinigen, Mel Wallace, VP, Clinical Supplies Management
9:50-10:25 EU MedTech Regulatory Workshop, led by Edward Staunton
10:25-10:50 EU MedTech Go-to-Market insights, Frederik Johanssen

See you at Herzog Towers, 6 Sadeh, TLV, for Europe MedTech Regulatory & GTM Workshop, with Edward Staunton, Fredrik Johansson and Mel Wallace.