Printer Friendly Version

    Mark Mansour has more than two decades of experience handling federal Food and Drug Administration (FDA) regulatory matters. He has significant experience working with clients in the food, pharmaceutical, medical device, dietary supplements and cosmetic industries to develop and implement strategies for regulatory approvals, compliance and enforcement actions, crisis management, rulemaking and public policy issues. He counsels corporations and organizations on how to negotiate effectively with government agencies in the United States and key global markets. 

    Mark is a leader in the development of regulatory pathway strategies for approvals in the United States and many international markets. He has been actively involved with industry and government to achieve solutions to issues such as the regulation of biotechnology and nanotechnology and also is active in domestic and international industry groups involving the key regulated industries. Throughout his seasoned career, he has taken a lead role in drafting industry comments in response to key rulemaking activities.

    Read More

    Find News, Events, Notable Matters, and More

    Showing Results for



    Please understand that your communications with Locke Lord LLP through this website do not constitute or create an attorney-client relationship with Locke Lord LLP. Any information you send to Locke Lord LLP through this website is on a non-confidential and non-privileged basis. Therefore, do not send or include any information in your email that you consider to be confidential or privileged.