Focused on helping start-ups and mid-size medical device companies interpret FDA regulations.
The journey to being able to legally distribute a medical device in today's complex market can be a long and expensive one, especially if you are a start-up, mid-size or international business. Misinterpreting the regulatory process can be an unwelcome delay and costly oversight. O'Connell & Myers has the knowledge and experience to navigate these regulatory pitfalls to help you get your device to market.
Book a call so we can discuss how I can help you.