Free PMS Plan Template for Medical Device Manufacturers
Stay compliant with MDR & ISO 13485 with a structured, easy-to-use Post-Market Surveillance plan.
What You’ll Get
This Post Market Surveillance (PMS) template includes:
A complete structure to build your PMS plan.
Sections aligned with MDR (EU) 2017/745 and ISO 13485.
Guidance on data collection, evaluation, and reporting.
Ready-to-fill fields for your product and documentation references.
Suitable for both legacy and MDR-compliant devices.
Why This Post Market Surveillance Template Matters
Save hours of documentation work.
Improve audit readiness and regulatory alignment.
Created by experts in MedTech compliance and documentation.
Benefits of using our PMS Plan Template:
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