FDA aims to give reviewers an inside view of medtech development

04/4/2013 | MassDevice.com (Boston)

As part of its Experiential Learning Program, the FDA will send reviewers at the agency's device center to tour medtech facilities in an effort to help them better understand the device-development cycle and the hurdles faced by manufacturers from development to clinical testing. The agency is inviting medtech companies to register as hosts for the tours.

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MassDevice.com (Boston)

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