Join MDIC, a unique public-private partnership committed to advancing medical device regulatory science. Collaborate with trusted partners, address complex challenges, and ensure the best in healthcare reach those in need.

2019年3月2日 · MDIC coordinates the development of methods, tools, and resources used in managing the total product life cycle of a medical device to improve patient access to cutting-edge medical technology.

MDIC can empower your innovation at every phase of the total product lifecycle. Explore the work happening within each of our programs to discover resources that will transform your company’s journey.

2025年3月10日 · Following the pilot study, MDIC found the MedAccred audit and accreditation program robust and comprehensive concerning the covered Sterilization processes combined with a thorough evaluation of the Quality Management System (QMS) requirements.

The MDIC IVD Clinical Evidence Framework provides a high-level overview that IVD manufacturers can use to make decisions on how to develop credible evidence of analytical and clinical validity, as well as clinical utility.

2025年2月10日 · Connecting you with breaking developments in medtech innovation, as well as opportunities to benefit from MDIC's tools and community, SIGHTLINE is a go-to inbox resource for the medical device industry and beyond.

Join the Medical Device Innovation Consortium (MDIC) and be part of a groundbreaking Public-Private partnership dedicated to advancing medical device regulatory science throughout the entire product life cycle.

MDIC’s Center for Manufacturing Innovation and Quality drives excellence across MedTech by serving as a hub for resources on the most innovative practices in quality, design, production, risk management, and so much more.

Are you looking to stay ahead of digital health trends, connect with industry leaders, and contribute to advancements in AI, cybersecurity, and software-based MedTech? Innovator Circles offer MDIC members an exclusive space to collaborate, share insights, and drive meaningful progress in digital health innovation and regulation.

2025年1月28日 · The Open Hand Initiative, led by MDIC in collaboration with the FDA and industry partners, showcases a groundbreaking approach to using real-world data (RWD) and real-world evidence (RWE) in regulatory submissions.