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Webinar - MDR Rule 14 Devices
  • Webinar
    Medical Devices

MDR Rule 14 Devices

Conformity assessment process and documentation requirements for submissions

Watch the Webinar View the Presentation

This Webinar:

  • Device and Drug Combinations in EU.

  • Introduction to BSI Medicinal team.

  • MDCG 2020-12 - MDR Conformity Assessment Process.

  • Competent Authority Assessment & Documentation Requirements.

Contributors

Conformity assessment process and documentation requirements for submission

Hear from Theresa Jeary as she explains more about the conformity assessment process for medical devices containing an ancillary medicinal substance.

  • Contributor

    Theresa Jeary

    Global Head - Medicinal & Biologics, BSI.

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