Our Team

  • Michael H. Cohen Founder

    Served as Assistant Professor of Medicine at Harvard Medical School and Adjunct faculty at Harvard School of Public Health, Author of 6 leading books on Health and Wellness Law, Recognized for his contribution to international health law and policy. Michael H. Cohen is a thought leader in health care law, pioneering legal strategies and solutions for clients in traditional and emerging healthcare markets.

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  • Randy Berholtz Of Counsel

    Randy specializes in providing corporate, securities, mergers and acquisitions, public and private financing, venture capital, corporate governance, commercial, licensing, commercial agreements, employment and real estate advice to life science, healthcare, alternative health and exercise companies and venture capital, angel groups and private equity firms in San Diego, Orange County, Los Angeles and Silicon Valley.

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  • Jessica Passman Of Counsel

    Jessica received her BA in Business & Finance from the University of Central Florida, and her JD (Cum Laude) from the University of Miami School of Law. After graduating from law school, she was an Associate Attorney at several top law firms, focusing on Commercial Real Estate, and outside general counsel to numerous clients in her own law practice.

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  • Alan Dumoff Project Attorney

    Alan Dumoff, JD, MSW has practiced law since 1988 with a special focus on the legal needs of integrative physicians and complementary and alternative (CAM) practitioners. A former acting director of the National Commission for the Certification of Acupuncturists, Mr. Dumoff assists physicians and CAM practitioners with a wide range of regulatory, insurance, and disciplinary issues,…

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  • Dennis M. Moore
    Dennis M. Moore Regulatory Consultant

    Dennis M. Moore is currently Chief Technical Expert and Managing Partner of Auk Technical Services LTD. He has 28 years of experience in medical device design, software design validation systems and evaluations, manufacturing software validation, training drug and device firms in all aspects of device and pharmaceutical manufacturing, and experience helping firms achieve compliance to FDA regulation and International Standards regulations. Mr. Moore has given numerous web seminars on GMP issues; has traveled the world putting out FDA compliance related fires and authored many documents on quality system inspection, FDA/CA narrative report compilation, drug quality systems and software auditing techniques.

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