This 3-part webinar series will take place on three Thursdays in May from 12.30 – 1.45pm GMT, covering the following areas:
• 05.05.22: Preparing your MedTech start-up for the USA: A highlight of key considerations for US market entry
• 12.05.22: US MedTech regulation: How to secure regulatory approval from the US Food and Drug Administration
• 19.05.22: Reimbursement and market access: How you can secure patient reimbursement from US medical insurers, Medicare and Medicaid, and addressing other market access issues.
At each webinar you will be provided with an introductory presentation by a legal expert, setting out practical advice and tips. This will be followed by an interactive discussion with a panel of founders who have successfully entered the US market, sharing their experience.
Join these webinars individually, or as a series.
Who should attend? Founders and senior executives of start-up and scale-up digital health and medical diagnostic and device companies.
The webinars are suitable for both early-stage start-ups, planning for the future, and later stage start-ups and scale-ups, who are closer to entering the US market.