Developing a new medical device is a challenging process. It requires a thorough understanding not only of the needs and requirements of your customer, but also of the regulatory environment in which you bring the product to market. While product development is the first step in bringing your product to market, the regulatory approval process for medical devices must be top of mind from the early stages as well. An FDA regulatory strategy developed at the beginning of the process makes your regulatory pathway easier. Learn more about what a regulatory strategy is and why itâ€™s so important.