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Simplimedica
  • Clinical Evaluation & Investigation Training Course

    Clinical Evaluation & Investigation Training Course

  • Introduction to Design Control and Risk Management Training Course

    Introduction to Design Control and Risk Management Training Course

  • Introduction to Regulations for Med-Tech Start Up Companies Training Course

    Introduction to Regulations for Med-Tech Start Up Companies Training Course

  • Introduction to Software as a Medical Device EN62304 Training Course

    Introduction to Software as a Medical Device EN62304 Training Course

  • Introduction to the EU IVDR Training Course

    Introduction to the EU IVDR Training Course

  • Introduction to the EU MDR Training Course

    Introduction to the EU MDR Training Course

  • Medical Device Auditing – Internal, External, Supplier Training Course

    Medical Device Auditing – Internal, External, Supplier Training Course

  • Process Equipment Validation (including software) Training Course

    Process Equipment Validation (including software) Training Course

  • Quality Management for Medical Devices: ISO 13485 Training Course

    Quality Management for Medical Devices: ISO 13485 Training Course

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  • SERVICES
    • REGULATORY AND QUALITY ASSURANCE SERVICES
    • CONSULTANT ON DEMAND
    • MARKET ACCESS, REGULATORY ROADMAP & GRANT-WRITING
    • RESOURCES
    • INTENDED USE STATEMENT
  • TRAINING COURSES
  • SHOP
    • BOOK CONSULTATION
    • TEMPLATES
      • EQUIPMENT VALIDATION
      • MEDICAL DEVICES
      • PHARMACEUTICALS
  • DIGITAL HEALTHCARE
  • NEWS
  • ABOUT
    • ABOUT SIMPLIMEDICA
    • SIMPLIMEDICA PODCASTS
    • INTERNSHIPS
    • SIMPLIMEDICA ON LINKEDIN
    • SIMPLIMEDICA ON YOUTUBE
  • CONTACT