Medical Devices


Regular Regulatory Support

Regular Regulatory Support (RRS) is our flexible support service that provides oversight of all development activities and adapts to the needs and resources of the company over time to ensure that they are aligned with the regulatory requirements.

Regulatory issues can arise when undergoing relevant and critical procedures during the development of a Medical Device (MD).

How can DDR help?

  • DDR will foresee and efficiently manage any objection or regulatory issue in critical moments, thus guaranteeing the optimal MD development.
  • DDR will support your company by attending meetings and discussions with Notified Bodies (NB) and the Medical Device Expert Group (MDCG), as well as by preparing and submitting specific documentation.

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