Regulatory Strategy Forum for Medical Devices

Knowing how to develop an effective global regulatory strategy is an essential skill for regulatory professionals. Successful global regulatory strategies maximize commercial opportunities for healthcare product manufacturers while minimizing company risk. By engaging in in-depth analysis and workgroup collaboration, you will gain a thorough understanding of ways to enhance your strategy and further your product’s success

  • The New Medical Device Regulation globally
  • Medical Device Single Audit Program (MDSAP).
  • Reprocessing of Medical Devices in the Light of the EU & US MDR
  • Medical Device Innovation Consortium (MDIC) Including the National Evaluation System for Health Technology (NEST).
  • Medical Device Harmonization Initiatives.
  • Software as a Medical Device
  • 3D Printing of Medical Devices

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