dijous, 29 de setembre del 2016

5 Steps to Medical Device Commercialization in the U.S.

intertek-whitepaper-september2016-smallSpeed your medical devices to market with this complimentary guide which takes you step by step through the process of submitting your medical devices for approval from the FDA.
As a leader in third party testing and certification, our industry experts developed this guide to simplify the complex process to submit your medical devices to the FDA and provide an in-depth understanding of all that is involved, including:

  • Classifying your device
  • Identifying the correct premarket submission
  • Preparing the premarket submission
  • Submitting to the FDA
  • Establishing a registration and device listing

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