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19-20 October 2021
Virtual EventDelivered in CEST time zone

Melanie Crystal
Sr. Manager, Clinical Evidence, Quality and Compliance at Medtronic


Melanie Crystal leads a team of Clinical Evidence Specialists responsible for clinical evaluations, publications, PMCF evidence generation and provides clinical quality oversight in Medtronic’s Gastrointestinal division. Melanie has held multiple clinical positions in medical device, IVD, and biologics industries and has over 20 years of experience in clinical research spanning numerous therapies and product approvals. Melanie currently chairs the Medtronic corporate workstream on clinical survey process and operational development, contributes to Medtronic’s EU MDR clinical sustainability efforts, and is very interested in developing alternative “real-world” clinical evidence strategies.

Agenda Sessions

  • The Reality of The EU MDR: Meeting the Bar of Sufficient Clinical Evidence