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  • Medical Foods: Practical Tips to Meet FDA Requirements for
    Claims and Quality

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Tuesday - Aug 27, 2013 10:00 AM
  • End Time:
  • Tuesday - Aug 27, 2013 11:00 AM
  • Location:
  • Online
  • This medical foods regulatory compliance training will explain the regulatory processes to designate and market a product as medical food. Common issues with FDA compliance will be discussed using case studies and potential solutions will be provided.

    Who will Benefit:
    This webinar will provide valuable information to:
    -Manufacturers of medical foods
    -Physicians and hospital personnel
    -Dietary supplement manufacturers
    -Marketing and Advertising Professionals
    -Regulatory affairs professionals
    -Research analysts in the medical foods industry
    -Executive management of medical foods manufacturing companies

    Instructor Profile:
    Dr. Mukesh Kumar, is a Washington DC-based consultant in regulatory affairs and quality assurance for manufacturers and developers of FDA-regulated products. He and leads the Regulatory Affairs and Quality Assurance departments at Amarex, a full service pharmaceutical product development company based in Germantown, MD. His key expertise is in regulatory affairs, clinical trials and multi-national project management for medicinal and diagnostic products. He has been involved in about 100 clinical trials in more than 40 countries, has made several hundred US FDA submissions, and arranged a number of meetings with the US FDA. In addition, he has had made regulatory submission in the EU and India. He has conducted GCP, GLP, GMP and GACP audits in the US and several countries in Europe and Asia. He has conducted numerous training workshops in FDA compliance related issues. He has authored numerous articles in peer-reviewed journals. He is a well known expert in global regulatory affairs and has been an invited speaker at several professional and academic organizations worldwide. Dr. Kumar is a PhD in Biochemistry and has worked as a research scientist at the NIH, Baylor College of Medicine, Houston, and premier institutions in India. He is a certified regulatory affairs professional by the Regulatory Affairs Professional Society, USA.
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