• Commercialization
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    • Reimbursement
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    • Medical Device Market Analysis
  • Medical Device Services
      • Quality Management
      • Quality Management Systems: ISO 13485
      • Quality manager
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      • Auditing for Quality Management Systems and Technical Files
      • Technical File
      • Medical Device Technical Files for EU CE Marking
      • Clinical Evaluation Reports (CER) under the EU MDR
      • Biological Evaluation Reports (BER) under the EU MDR
      • FDA Approval Process for Medical Devices
      • Consulting
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      • European Authorized Representative
      • Medical Device Testing: ISO 10993
      • Medical Device Testing: IEC 60601
      • Medical Device and Quality Management Training
  • CRO
    • CRO Services – Project Management
    • CRA and Monitoring
    • Auditing Services and Quality Management for Clinical Trials
    • Good Laboratory Practice (GLP) Studies
  • IPR
  • Product & Compliance
    • Development of Medical Device Software
    • Cyber Resilience Act (CRA) Services
    • AI Act (Artificial Intelligence Act) Services
  • Blog
  • Contact details

2024

Medical Device and Quality Management Training by MDS Denmark

by adminReaktio | Nov 7, 2024 | Medical Device Services

Our Medical Device and Quality Management Training Covers QMS Fundamentals and Implementation We provide structured training on the principles, setup, and ongoing maintenance of a compliant Quality Management System (QMS) based on ISO 13485. Topics include QMS...

ISO 10993 Medical Device Testing by MDS Denmark

by adminReaktio | Nov 7, 2024 | Medical Device Services

How our ISO 10993 Biocompatibility Testing Services compliment your Biological Evaluation Biological Evaluation Plan (BEP) We begin by developing a Biological Evaluation Plan (BEP) which reviews the device and its materials, identifies potential biological risks, and...

IEC 60601 Medical Device Testing by MDS Denmark

by adminReaktio | Nov 7, 2024 | Medical Device Services

Ensure Electrical Safety with IEC 60601 Testing Services Foundational Standard IEC 60601-1 Compliance The IEC 60601-1 standard is the cornerstone of the series, setting the general requirements for basic electrical safety and essential performance. We provide thorough...

European Authorized Representative (EC-Rep)

by adminReaktio | Nov 7, 2024 | Medical Device Services

Key Aspects of European Authorized Representative (EC-Rep) Services Representation for Non-EU Manufacturers We act as your official representative (EC-Rep) within the European Union, a mandatory requirement for non-EU manufacturers under the EU Medical Device...

Quality Assurance and Regulatory Consulting

by adminReaktio | Nov 7, 2024 | Medical Device Services

Elevate your Quality Assurance and Regulatory Affairs with our help Technical Documentation Management Compiling, reviewing, and updating technical files for medical devices, medical device software, and in vitro diagnostic devices to ensure full regulatory...
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MDS Denmark

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CONTACT US

+45 2712 4712
Kristian@mdsdenmark.dk