$247 — Standard Tier

Document Control Procedure Toolkit: FDA 820.40 + ISO 13485 Templates

Document Control Procedure Toolkit: FDA 820.40 + ISO 13485 Templates - complete templates for medical device compliance.

Get the Toolkit — $247

7-day money-back guarantee • One-time purchase • Instant download

What's Included

Document Control Procedure (21 CFR 820.40 + ISO 13485 Cl. 4.2)
Document Change Request Form
Master Document List Template
Document Review and Approval Log
Obsolete Document Handling SOP
Training Acknowledgment Form

Benefits

Fully compliant templates ready for regulatory submissions
Saves 20+ hours vs building from scratch
Audit-ready documentation
Used by 500+ device manufacturers

Is This For You?

This toolkit is designed for teams facing these challenges:

FDA 483 observations for missing procedures
No standardized process across product lines
Auditors citing documentation gaps
Starting from blank pages

Who This Is For

QA/RA managers in medical device companiesCompanies preparing for FDA inspection or ISO 13485 auditRegulatory consultantsStartups building QMS from scratch

Frequently Asked Questions

What format are the documents?

All documents are editable Word/Markdown templates ready for direct QMS use.

Is this FDA and ISO 13485 compliant?

Yes, all templates are aligned with current FDA and ISO 13485:2016 requirements.

Ready to Get Started?

Download immediately after purchase. All templates are editable Word and Excel files.

Get the Toolkit — $247

7-day money-back guarantee