In The News

Cross-Practice Team Authors “Physician’s Guide to Commercializing a Medical Device Invention”

Practices: Health Care, Life Sciences, Intellectual Property, Intellectual Property Transactions, Digital Health, Health Care Transactions, Health Information Technology & Electronic Health Records, FDA Regulatory

Bringing together several different areas of the firm’s expertise, a team of Ropes & Gray lawyers authored a Practice Resource in the October issue of the American Health Lawyers Association’s Journal of Health & Life Sciences Law titled “Building a Better Mousetrap: A Physician’s Guide to Commercializing a Medical Device Invention.”

An AHLA Practice Resource is a how-to guide for lawyers. This one addresses the key steps a lawyer representing a physician inventor would take to bring a medical device to commercialization, including protecting and managing IP, forming a business and securing funds, FDA approval or clearance, FDA and anti-kickback restrictions on marketing, and third-party payer coverage and reimbursement.

The guide was written by health care partner Tom Bulleit (Washington, D.C.), IP transactions partner Megan Baca (Silicon Valley), life sciences associate Brad Flint (Boston), health care associate Katherine Sullivan (Washington, D.C), and corporate practice associate Beibei Sun (Boston). Co-authors also include Abram Barth, now Senior Regulatory Counsel at GRAIL, Inc. (when the article was written, an associate in the firm’s life sciences practice) and Gelvina Rodriguez Stevenson, Associate General Counsel at the Children’s Hospital of Philadelphia.

Cookie Settings