|Do you have a medical device you want to commercialize? Do you understand the true costs of development, the resources required, and the time it takes to bring a product to market?
Often, developing a medical device can become more expensive and time consuming than expected. More often, companies struggle with the regulatory pathways for a medical device because of the ambiguity and complexity of the process, coupled with the pre-clinical and clinical testing requirements. Additionally, companies often fail to understand the needs of investors and strategic partners.
In addition to an update on the FDA medical device industry guidance, this session will cover:
• Reducing the risk for late-stage failures and post-authorization action
• Understanding what goes into a medical device budget and what it costs
• Developing a realistic and successful project plan
• Planning and budgeting for contingencies
Thursday, March 26th at noon | Virtual Meeting