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Bill Kurani
Head and Director of Regulatory Affairs & Quality Assurance at Agilent Technologies, USA


Mr. Bill Kurani – MSRA (SDSU), MSEE (LSU), BC (Stanford) has extensive experience in the area of regulatory affairs and quality assurance of medical device including regulatory clearances from FDA, EU as well as other global regulatory bodies. Mr. Kurani has helped several medical device companies implement successful product design, validation and manufacturing process programs. He has done hazard and risk analysis on many aspects of the medical device design and manufacturing process. Mr. Kurani has setup successful post market surveillance and vigilance systems adhering to FDA, EU and ROW regulations in several companies. Mr. Kurani currently actively involved in development and commercialization of Next Generation Sequencing product. Grande.

Agenda Sessions

  • CANADA Registration in Canada: Navigating Mandatory MDSAP and Evolving Regulations

  • JAPAN Shortcuts to Swift and Cost-Effective Registration in Japan