---
title: "Free quality agreement review tool"
description: "Free AI review of a pharma or medtech quality agreement: responsibilities matrix, GMP, change control, deviations, CAPA, batch release, audits."
canonical: "https://contracko.com/tools/quality-agreement-review"
---
# Free quality agreement review tool

Source: https://contracko.com/tools/quality-agreement-review

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# Free quality agreement review tool

Upload a quality agreement (QAG) and get instant AI analysis of the roles-and-responsibilities matrix, GMP compliance, change control, deviations and CAPA, batch release, audits and inspections, complaint handling, and regulatory obligations.

Upload your contract to start your free analysis

Drag and drop your contract here, or browse files

PDF or DOCX, max 50MB, up to 100 pages

What we'll analyze

Our AI engine reviews your contract and extracts key insights across multiple dimensions:

Risk assessment

Overall risk score with specific concerns

Key dates

Start, end, renewal, and notice deadlines

Obligations

Your duties and counterparty requirements

Financial terms

Pricing, payment terms, and penalties

Red flags

Unusual or concerning clauses

Liability & indemnity

Caps, exclusions, and indemnification

Your privacy, guaranteed

Enterprise-grade encryption

Never used for AI training

GDPR compliant

Deleted after analysis

## Frequently asked questions

Common questions about our quality agreement review

- **Q:** What does this quality agreement review tool check?
  **A:** It analyzes the roles-and-responsibilities matrix between the sponsor and contract manufacturer, GMP-compliance obligations, change-control procedures, deviation and CAPA handling, batch-record review and batch release (who has final disposition authority), audit and regulatory-inspection rights, complaint and adverse-event handling, and the allocation of regulatory responsibilities. Both parties’ obligations are extracted and listed.

- **Q:** Does it map the roles-and-responsibilities matrix and batch release?
  **A:** Yes. It surfaces who is responsible for each GMP activity in the responsibilities matrix and identifies who holds final batch-release and disposition authority, flagging ambiguous or shared responsibilities that cause the most disputes between a sponsor and a CMO.

- **Q:** How does it handle change control, deviations, CAPA and audits?
  **A:** It extracts the change-control process and notification obligations, how deviations and out-of-specification results are investigated and how CAPAs are managed, and the audit and regulatory-inspection rights (frequency, for-cause audits, and the duty to notify the other party of a regulatory inspection).

- **Q:** How long does the quality agreement analysis take?
  **A:** Most quality agreements are analyzed in under 30 seconds.

- **Q:** What file formats can I upload?
  **A:** PDF and Word (DOCX) files are both supported.

- **Q:** Is my quality agreement data secure?
  **A:** Yes. Your document is transmitted over TLS encryption, processed by AI providers under terms that exclude training on your data, and deleted from our servers within 24 hours.

## Try our other contract analysis tools

Specialized analyzers for specific contract types with tailored insights and recommendations.

### [Manufacturing agreement review](https://contracko.com/tools/manufacturing-agreement-review)

### [OEM agreement review](https://contracko.com/tools/oem-agreement-review)

### [Tolling agreement review](https://contracko.com/tools/tolling-agreement-review)

[View all contract analysis tools](https://contracko.com/contract-analysis-tools)

## Get started with Contracko

Take the hassle out of contract management. Contracko empowers you to stay organized, on time, and in control. Start simplifying today.

[Start 7-day free trial](https://app.contracko.com/register?appLanguage=en)

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