To commercialize innovative products, medical device developers must address issues such as regulatory clearance or approval, patents, financing, manufacturing, and distribution in an increasingly complex global market. We help clients mitigate risks and pursue opportunities through timely, effective counsel on matters relating to the entire life cycle of Medical Devices. From inception and approval to debut and product maturity, you will benefit from guidance that reflects your business strategies and legal needs.
Our clients include local, regional, and global developers, manufacturers of Medical Devices, researchers, investors, and trade associations. Many of our lawyers and regulatory science professionals have worked for regulatory agencies and in private industry, and have advanced degrees in relevant scientific or technological areas. We advise clients on all aspects of regulation local, national, and international regulatory entities. We also work with colleagues in our Life Sciences practice, ranked as a global leader, along with dedicated teams in the areas of regulatory compliance, health coverage, reimbursement, and pricing, fraud and abuse prevention, legislation and policy, intellectual property, financing, product liability, litigation and investigations, licensing and technology transfer, international trade, and pharmaceuticals and biotechnology.