---
description: Learn more about MedDeviceAudit price, benefits, and disadvantages for businesses in Australia. Read reviews from verified users and discover similar tools that fit your business needs.
image: https://gdm-localsites-assets-gfprod.imgix.net/images/capterra/og_logo-e5a8c001ed0bd1bb922639230fcea71a.png?auto=format%2Cenhance%2Ccompress
title: MedDeviceAudit Cost & Reviews - Capterra Australia 2026
---

Breadcrumb: [Home](/) > [Compliance Software](/directory/30110/compliance/software) > [MedDeviceAudit](/software/1095498/MedDeviceAudit)

# MedDeviceAudit

Canonical: https://www.capterra.com.au/software/1095498/MedDeviceAudit

> AI-powered FDA QMSR 2026 \&amp; ISO 13485 compliance auditing for medical device manufacturers. Evidence-anchored findings. First audit free
> 
> Verdict: Rated \*\*\*\* by 0 users. Top-rated for **Overall Quality**.

-----

## Overview

### Who Uses MedDeviceAudit?

Medical device manufacturers, QA Managers, and Regulatory Affairs professionals navigating FDA QMSR 2026, ISO 13485, and IEC 62304 compliance. Ideal for Class I, II, and III device companies preparing

## About the vendor

- **Company**: MedDeviceAudit

## Commercial Context

- **Starting Price**: USD 495.00
- **Pricing model**: Flat Rate (Free version available)
- **Target Audience**: Self Employed, 2–10, 11–50, 51–200, 201–500
- **Deployment & Platforms**: Cloud, SaaS, Web-based
- **Supported Languages**: English
- **Available Countries**: Angola, Argentina, Aruba, Australia, Austria, Bahamas, Bahrain, Belgium, Bermuda, Bosnia and Herzegovina, Botswana, Brazil, Bulgaria, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, Croatia and 68 more

## Features

- Audit Management
- Compliance Tracking

## Support Options

- Email/Help Desk
- FAQs/Forum
- Chat

## Category

- [Compliance Software](https://www.capterra.com.au/directory/30110/compliance/software)

## Alternatives

1. [ManageEngine Network Configuration Manager](https://www.capterra.com.au/software/172274/network-configuration-manager) — 4.5/5 (283 reviews)
2. [Connecteam](https://www.capterra.com.au/software/153140/connecteam) — 4.6/5 (5203 reviews)
3. [Scrut Automation](https://www.capterra.com.au/software/1052809/scrut) — 4.9/5 (139 reviews)
4. [Account Ability](https://www.capterra.com.au/software/154484/account-ability) — 4.9/5 (219 reviews)
5. [MasterControl Quality Excellence](https://www.capterra.com.au/software/148577/mastercontrol) — 4.5/5 (534 reviews)

## Links

- [View on Capterra](https://www.capterra.com.au/software/1095498/MedDeviceAudit)

## This page is available in the following languages

| Locale | URL |
| en | <https://www.capterra.com/p/10040862/MedDeviceAudit/> |
| en-AE | <https://www.capterra.ae/software/1095498/MedDeviceAudit> |
| en-AU | <https://www.capterra.com.au/software/1095498/MedDeviceAudit> |
| en-CA | <https://www.capterra.ca/software/1095498/MedDeviceAudit> |
| en-GB | <https://www.capterra.co.uk/software/1095498/MedDeviceAudit> |
| en-IE | <https://www.capterra.ie/software/1095498/MedDeviceAudit> |
| en-IL | <https://www.capterra.co.il/software/1095498/MedDeviceAudit> |
| en-IN | <https://www.capterra.in/software/1095498/MedDeviceAudit> |
| en-NZ | <https://www.capterra.co.nz/software/1095498/MedDeviceAudit> |
| en-SG | <https://www.capterra.com.sg/software/1095498/MedDeviceAudit> |
| en-ZA | <https://www.capterra.co.za/software/1095498/MedDeviceAudit> |

-----

## Structured Data

<script type="application/ld+json">
  {"@context":"https://schema.org","@graph":[{"name":"Capterra Australia","address":{"@type":"PostalAddress","addressLocality":"Sydney","addressRegion":"NSW","postalCode":"2060","streetAddress":"Level 18 40 Mount Street North Sydney NSW 2060 Australia"},"description":"Capterra Australia helps millions of people find the best business software with user reviews, ratings and price comparisons.","email":"info@capterra.com.au","url":"https://www.capterra.com.au/","logo":"https://dm-localsites-assets-prod.imgix.net/images/capterra/logo-a9b3b18653bd44e574e5108c22ab4d3c.svg","@id":"https://www.capterra.com.au/#organization","@type":"Organization","parentOrganization":"G2.com, Inc.","sameAs":["https://twitter.com/Capterra","https://www.linkedin.com/company/capterra/","https://www.youtube.com/channel/UCjRCDmEibpHwyX3m2b3y80w"]},{"name":"MedDeviceAudit","description":"MedDeviceAudit is an AI-powered compliance auditing platform built specifically for medical device manufacturers. It audits technical files against FDA QMSR 2026 (21 CFR Part 820), ISO 13485:2016, IEC 62304, and ISO 14971 — returning evidence-anchored findings grounded in your actual documents with SHA-256 verified citations, literal quotes, and page references.\nEvery finding is mapped to the exact regulatory clause it evaluates — not AI summaries or assumptions. Gaps are prioritized by severity (Critical, Major, Minor) with ready-to-use draft remediation language and step-by-step corrective actions included for every finding.\nZero-retention data policy — uploaded documents are permanently deleted after every audit. Never stored, never shared, never used to train AI. Only your audit report is saved to your private dashboard.\nWorks for Class I, II, and III medical devices including SaMD. Supports PDF files up to 50MB. Audits complete in under 5 minutes. First audit always free with no c","image":"https://gdm-catalog-fmapi-prod.imgix.net/ProductScreenshot/8c00da70-be5a-4620-88b2-d25bf86116c4.png","url":"https://www.capterra.com.au/software/1095498/MedDeviceAudit","@id":"https://www.capterra.com.au/software/1095498/MedDeviceAudit#software","@type":"SoftwareApplication","applicationCategory":"BusinessApplication","publisher":{"@id":"https://www.capterra.com.au/#organization"},"offers":{"price":"495","@type":"Offer","priceCurrency":"USD"},"operatingSystem":"Cloud"},{"@id":"https://www.capterra.com.au/software/1095498/MedDeviceAudit#faqs","@type":"FAQPage","mainEntity":[{"name":"What Is MedDeviceAudit?","@type":"Question","acceptedAnswer":{"text":"MedDeviceAudit is an AI-powered compliance auditing platform built specifically for medical device manufacturers. It audits technical files against FDA QMSR 2026 (21 CFR Part 820), ISO 13485:2016, IEC 62304, and ISO 14971 — returning evidence-anchored findings grounded in your actual documents with SHA-256 verified citations, literal quotes, and page references.Every finding is mapped to the exact regulatory clause it evaluates — not AI summaries or assumptions. Gaps are prioritized by severity (Critical, Major, Minor) with ready-to-use draft remediation language and step-by-step corrective actions included for every finding.Zero-retention data policy — uploaded documents are permanently deleted after every audit. Never stored, never shared, never used to train AI. Only your audit report is saved to your private dashboard.Works for Class I, II, and III medical devices including SaMD. Supports PDF files up to 50MB. Audits complete in under 5 minutes. First audit always free with no c","@type":"Answer"}},{"name":"Who Uses MedDeviceAudit?","@type":"Question","acceptedAnswer":{"text":"Medical device manufacturers, QA Managers, and Regulatory Affairs professionals navigating FDA QMSR 2026, ISO 13485, and IEC 62304 compliance. Ideal for Class I, II, and III device companies preparing","@type":"Answer"}}]},{"@id":"https://www.capterra.com.au/software/1095498/MedDeviceAudit#breadcrumblist","@type":"BreadcrumbList","itemListElement":[{"name":"Home","position":1,"item":"/","@type":"ListItem"},{"name":"Compliance Software","position":2,"item":"/directory/30110/compliance/software","@type":"ListItem"},{"name":"MedDeviceAudit","position":3,"item":"/software/1095498/MedDeviceAudit","@type":"ListItem"}]}]}
</script>
