ISO 13485

Record Retention 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 defines, for every type of quality record produced by the your organisation QMS, who owns it, where it is kept and how long it must be retained before it may be disposed of.

What's Inside

  • Basis for Retention Periods
  • Retention Classes
  • Device Lifetimes
  • Register of Records
  • QMS Documents and Stand-Alone Records
  • Records Created on Procedure Forms
  • Other Records
  • Storage, Protection and Retrieval

ISO 13485 Alignment

Supports ISO 13485:2016 requirements, including Clause 4.2.5. 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