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Archives: News

As healthcare professional or institute – what does the new medical device regulation change for you?

How to determine what Post Market Clinical Follow-up activities to initiate?

Case Story – Investigator Initiated Studies

Are you our new CRA?

The new Medical Device Regulation – and its impact on innovation

Are your investigator and site ready for an FDA inspection? – Part 2

Are your sites prepared for FDA inspection of your clinical investigations in EU?

MEDDEV 2.7/1 Rev 4 Clinical Evaluation: Are you ready to update your clinical evaluation report.

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  • Koebmagergade 53, 1.
    DK-1150 Copenhagen K.

  • +45 56 64 10 10
  • info@qmed-consulting.com
Our services
  • Clinical Affairs
  • Strategic Consulting
  • Regulatory Affairs
  • Quality Management
  • Reimbursement & Market Access
  • Clinical Development
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About us

Qmed Consulting is a global full-service Contract Research Organization (CRO) managing Clinical Studies from Copenhagen, Denmark. We also provide Strategic Consulting services in connection with medical device approval as well as best-in-class expertise in clinical affairs, regulatory affairs, quality management and commercial healthcare. 

Qmed Consulting is an ISO 9001:2015 & 14155:2020 certified company.

Proud sponsors of Red Cross and Mothers Aid.