October 10, 2023
The FDA recognizes the importance of human factors engineering in the design and development of medical devices, including clinical support software. Designing clinical tools around human factors takes into account human capabilities, limitations and characteristics to protect the wellbeing of people and to minimize the risk of design-induced human performance issues. The regulatory pathway for clinical support software can vary based on intended use, risk level and complexity of the software. Within these pathways, Human Factors data is an integral part of your product development and data to support your regulatory submission.
September 14, 2023
Celebrate Invention is an annual event that honors University of Michigan inventors and the growing impact of U-M innovations.
March 9, 2023
Aspiring to Impact is a networking group created by Innovation Partnerships to bring together faculty and researchers interested in closing the gap in women’s leadership in entrepreneurial communities.
February 7, 2023
Join us for discussion and insights on FDA Regulation of Clinical Decision Support Software & Artificial Intelligence and Machine Learning (AI/ML). Featuring Pamela Forrest and Christina Kuhn from Covington & Burling LLP.
February 6, 2023
Brief Abstract Deadline: February 23, 2023
October 6, 2022
Innovation Partnerships is hosting a one-of-a-kind webinar on open source software licensing strategy. Heather Meeker is a thought-leader in software licensing, and open source licensing strategy & business models. She is also a founding partner of OSS Capital, a firm focused on early-stage investment in commercial open source companies.