The Medical Device Innovation Consortium (MDIC) brings together medical device stakeholders and leverages their expertise, resources, and data to facilitate the creation of methods, tools, approaches, and standards that will assist in developing safe and effective medical technologies for patients. These resources are aimed at addressing strategic, technical issues that affect the industry and the public.

By providing comments to our draft resources, the public can help MDIC obtain a wider span of knowledge that can be taken into consideration when addressing regulatory science and public health needs. We appreciate receiving input as we work to advance the medical device regulatory process to reduce the time and cost of device development, assessment, and review, and to advance the safety and effectiveness of medical devices throughout their total product life cycle.