EE Times Medical Device Virtual Conference
Panel Discussion: Best Practices for Boosting Time to Market
Product development is getting more complex, which means FDA approval can take longer. Missing a window of opportunity for a product launch can make the difference between corporate success and failure. There are many options available to help companies speed product development without risking FDA approval. Join MKS's Steve Mostello along with other experts in the medical device industry for this session that will discuss proven best practices that are adopted by medical system companies to lower the risk of product development. Register for the virtual conference and get access to this session, the exhibits and more.