Pilot initiative will test tools for streamlining medtech regulatory processes

08/21/2014 | MassDevice.com (Boston)

The FDA has released guidelines governing its pilot program to develop tools for streamlining the premarket review and registration process. The agency will seek participants in the Medical Device Development Tools Pilot Program starting next month. Tools that might work for the pilot include those that examine how devices affect public health or tools for speeding development and commercialization of devices, the guidance states.

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MassDevice.com (Boston)

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