The medical device (MD) market has undergone profound changes over the past twenty years, under the combined effect of three factors of change: the considerable development of technologies, the strengthening of European and national requirements in terms of health safety, and growing economic constraints on reimbursement spending.
In this context, medical device manufacturers must be able to anticipate very early in the development of their product the requirements to meet to obtain not only CE marking but also manage a successful product pathway on the market.
Our panel of expert speakers will give an overview of the different routes to market to sell your solution in France and look through the DOs and DON’Ts when working with a French partner.
10.00 – Welcome & Introduction, Julie Lebouleux, Senior Adviser, Health & Life Sciences, Department for International Trade, British Embassy in France
10.05 – Accessing the French market: reimbursement schemes & financial incentives, Anouk Trancart, Market Access Director, SNITEM
10.15 – The pharmacy market (OTC), Rayan Arsan, Sales Manager, ACLsanté
10.25 – The Private Hospital market, Béatrice Samyn, Director of Medical Department, CACIC
10.35 – The Public Hospital market, Louis Potel, Head of international affairs & Innovation project coordinator, RESAH
10.45 – Best Practice sharing – DOs and DON’Ts in working with a French partner, Eric Del Cotto, General Manager South of Europe and North Africa, Owen Mumford France
10.55 – Q&A and close
Closing date: 14 April