Record Retention Procedure

$49.00
$49.00
Unavailable
per item
The ISO 13485:2016 compliant Record Retention Procedure provides guidelines for the retention of all confidential, electronic, quality and archived records and supportive documentation per applicable standards and regulations.
  • ISO 13485:2016 Compliant
  • FDA QSR Compliant
  • ​Includes Retention Period Table
  • MS Word Format
  • ​Digital Content - Instant Download
​
SKU:

ISO 13485 Record Retention Procedure

​The ISO 13485:2016 compliant Record Retention Procedure provides guidelines for the retention of all confidential, electronic, quality and archived records and supportive documentation per applicable standards and regulations.

Record Retention Procedure Compliance

The Record Retention Procedure is ISO 13485:2016 and FDA 21 CFR Part 820 compliant.
ISo 13485 Record Retntion Procedure
Record Retention Procedure

Customer's also viewed

ISO 13485 Document Control Procedure Bundle

$399.00
The Document Control Procedure Bundle includes six (6)  ISO 13485 quality system procedures relating to the creation, maintenance, distribution, format and retention of all controlled documents within an organization.  All procedures are ISO 13485:2016 and FDA QSR compliant.
  • ISO 13485:2016 Compliant
  • FDA QSR Compliant
  • Includes Related Forms
  • MS Word Format
  • ​Instant Download Digital Content
view

Medical Device Quality Management System | DESIGN PLUS

$2,699.00

The DESIGN PLUS Quality Management System (QMS) is configured for companies engaged in research and development of medical devices but perform no manufacturing (Specification Developers). The Design Plus QMS system is configured for companies desiring ISO 13485:2016 certification and FDA QSR compliance. Products installed in 46 countries and growing!​

  • Quality Management System Manual
  • 46 Procedures and Related Forms (MS Word and Excel)
  • ISO 13485:2016 and FDA QSR Compliant
  • MDR EU 2017/745 Compliant​​​​​
  • Digital Content - Instant Download 
view

Medical Device Quality Management System | MANUFACTURING

$2,899.00

The Medical Device Quality Management System | MANUFACTURING product is designed for companies engaged in both product development and the manufacture of medical devices. The system is rich in content and provides detailed instruction governing research and development, manufacturing and post commercialization activities. The system is configured for companies desiring ISO 13485:2016 certification and FDA QSR compliance. Products installed in 46 countries and growing!​

  • Quality Management System Manual
  • 60 Procedures and Related Forms (MS Word and Excel)
  • ISO 13485:2016 and FDA QSR Compliant
  • MDR EU 2017/745 Compliant​​​​​
  • Digital Content - Instant Download ​
view

Medical Device Quality Management System | MANUFACTURING PLUS

$3,599.00

The Medical Device Quality Management System | MANUFACTURING PLUS System is our "top line" QMS product configured for companies engaged in the design and manufacture of medical devices seeking ISO 13485:2016 certification and FDA QSR compliance. Products installed in 46 countries and growing!​

  • Quality Management System Manual
  • 72 Procedures and Related Forms (MS Word and Excel)
  • ISO 13485:2016 and FDA QSR Compliant
  • MDR EU 2017/745 Compliant​​​​​
  • Digital Content - Instant Download ​
view
Copyright © 2010-2024
  •