Medical Device Regulations and Guidance Training, Compliance Best Practices and Standards

Medical device regulations and guidance training through webinars, in-person seminars, standards and best practices. Learn from renowned experts about current and upcoming FDA medical device regulations and guidance - 510(k) submissions, Medical Devices Directive, CE mark and EEC Directive, Clinical Evaluation Reports (CER's), New Approach Directives (NAD), CE-mark compliance, Premarket Approval (PMA) agreement, etc.
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