Effective product development in the medical device and biotechnology industries requires a company to understand both the intellectual property (IP) and Food and Drug Administration (FDA) implications of its work. This seminar is designed to help engineers, designers and project managers efficiently navigate the medical device or biotechnology product-development process. Companies that integrate knowledge of FDA regulatory requirements and IP portfolio management into their product development processes are more likely to experience success.
Specifically, this seminar will focus on:
- Understanding the basics of patent and FDA regulatory application processes
- Identifying key intersection points between patent application and FDA regulatory processes
- Implementing practical workforce tools for successful product development.