Χρήσιμα έγγραφα

• European regulatory framework
  • European Regulations and Directives
  • Harmonised standards
  • Guidelines
• HTCert documents
  • Regulations for the certification
    • General Terms and Conditions for Certification of Quality Management Systems
    • General Terms and Conditions for Certification of Medical Devices
    • Technical Documentation for Medical Devices – Guidance for submission
    • Rules for the use of Certification, Certificate and Certification Mark