The panel of experts will explore various ways that companies developing and manufacturing medtech devices can make good, strategic decisions, that future proof them against changing regulatory and market conditions. The panel will discuss:
- How to safely push the regulatory boundaries and work with the FDA at the design stage to keep your options open when it comes to commercialization.
- How to design a product that is optimized for the transfer to manufacturing stage.
- Tips and tricks for selecting and managing the right Contract Manufacturer for your product.
- How to manage uncertainty and volatility in the demand for your product volumes.
The panel will also address the key risks facing medtech manufacturers at the moment and discuss whether strategies such as dual sourcing and supply chain redundancy are effective.