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Good Manufacturing Practice


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  Registration of Medical Devices in Italy

  Clinical Trial Services

  Process Validation & Product Safety
  Acting as European Authorized Representiative for medical device and in-vitro diagnostics manufacturer located outside the European Union.
  Acting as Legal Representative for clinical trials of medicinal products according to Directive 2001/20 EC.
MT Promedt Consulting GmbH   •   Altenhofstraße 80   •   D-66386 St. Ingbert   •   Tel.: +49 (0) 6894-581020   •   Fax: +49 (0) 6894-581021   •   eMail: info(at)mt-procons.com
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