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Guide to achieving a clinical evaluation of medical technology

Your guide to achieving clinical evaluation

Clinical evidence is an essential part of developing a medical device or process. This is often a lengthy and costly part of product development where safety needs to be balanced with the innovation of potential breakthrough technology.

Find out about the scope of medical device regulation and the ideal approach to achieve healthcare market adoption in our guide covering:

  • The regulatory responsibility of medtech companies, including CE marking
  • Clinical trials for non-CE marked devices
  • Evidence for medtech adoption
  • Continuing post-market clinical follow-up

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