Site Map

• Home
• Qserve Consultancy
  • About Us
    • Our Team
    • Mission
    • Achievements
    • Address
    • Directions
    • Achievements
  • Services
    • CE Marking consultancy and CE Marking Services
    • Preclinical Studies
    • Strategic regulatory Consulting
    • Risk Management (ISO 14971)
    • ISO 13485:2003, Medical devices Quality management systems
    • Audits EN ISO 13485:2003 and EN ISO 9001:2000
    • Biocompatibility for Medical Device
    • Medical device product validation
    • Distributor Search::European/USA Distributor Research for Medical Devices Manufacturers
    • European Authorized Representative Services By Obelis O.E.A.R.C.
    • 510K, IDE, PMA submissions
    • US Agent and Official Correspondent Services
  • Training
    • Regulatory Affairs
    • Quality Management Systems
      • ISO 13485:2003 Quality Management systems (2 days)
      • ISO 13485:2003 Quality Management systems (1 day)
      • ISO 13485: 2003 for Managers
      • CE Marking of Medical Devices Conform the European Medical Device Directive(s)
      • Introductory course/workshop Medical Device Directive a Better Understanding
    • Auditing
      • Internal Auditor Training
      • Internal Audit Training
    • Risk Management Training
      • Risk management analysis (2 days)
      • Risk management analysis (1 day)
    • Medical Device Design and Device Development
    • Training: Biological Safety Evaluation-ISO 10993 Series by the Experts of Qserve Consultancy
    • Regulatory Affairs Training/ Quality Mangement Training Courses Schedule for 2006
  • News
    • Medical Exhibitions
    • Special Events
  • Links
    • OneLink:OneSolution
    • Industry Links
    • Sites of Interest
  • Alliances
  • Contact Us
  • Medical Articles
• Qserve America
  • About Us
    • Our Team
    • Mission
    • Achievements
  • Services
  • Training
  • News
  • Links
    • OneLink:OneSolution
    • Industry Links
    • Sites of Interest
  • Alliances
  • Contact Us
• Qserve Support
• Sitemap
• Terms