ISO 13485

Training Register

Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.

Fully Customizable Audit Ready Instant Download
Standard
ISO 13485
Document Type
Register
Format
DOCX
Language
English
Tags
ISO 13485, Medical Devices, Register

This register is the central record of all training delivered to personnel of your organisation whose work affects product quality, of the effectiveness of that training, and of each person’s qualification to perform high-risk tasks.

What's Inside

  • Summary Dashboard
  • Personnel List
  • Training Event Log
  • Individual Training Records
  • Qualification and Authorisation Status — High-Risk Tasks
  • Overdue and Retraining Tracker
  • External Training and Certificates
  • Review and Approval

ISO 13485 Alignment

Supports ISO 13485:2016 requirements, including Clause 6.2. It fits with the rest of the QEHS Vault ISO 13485 document set.

Format

Supplied as a fully editable Microsoft Word (.docx) file. Add your organisation’s name, logo and details, then use it straight away. Instant download after purchase.

Key Benefits

  • Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements