Navigating FDA Regulations for Medical Devices

​Join our upcoming webinar where we delve into essential topics for medical device companies, starting with the role of FDA Regulatory Counsel, who navigate the complexities of regulatory compliance and strategy. We will provide an overview of the FDA regulatory framework for medical devices, highlighting key pathways. The webinar will also explore the integration of digital health technologies, focusing on devices using artificial intelligence (AI) and machine learning (ML) within the FDA’s regulatory landscape.

​Featuring speaker, Blake Wilson.

​Blake Wilson is a Partner in Hogan Lovells’ FDA Regulatory group.  He holds a JD from the University of Pennsylvania and a MS in biostatistics from Columbia University.  His legal practice focuses on FDA’s premarket approval process for devices/drugs/biologics, oversight of clinical trials including BIMO audits, as well as navigating changes in laws or regulations that govern the life sciences industry.  In this capacity, Blake advises extensively on novel products, including digital health technologies and products that incorporate AI/ML.