QMSR enforcement is now active. Are you inspection-ready? Check Your Readiness

Design Partner Application

Become a Design Partner

For medical device manufacturers evaluating documentation alignment, inspection readiness, and compliance operations.

Estimated time: 5 minutes Reviewed within: 1 business day Mutual NDA before documentation review No obligation
1
Company
Information
2
Primary
Contact
3
Current
Environment
4
Current Compliance
Priorities
5
Review &
Submit

Company Information

This helps us tailor the program to organizations of your size.

Select the category that best describes your primary products.

Primary Contact

We'll use this to follow up about your application.

Current Environment

The system you rely on for quality and compliance processes.

Current Documentation Systems (select all that apply)

Current Compliance Priorities

0/1000

Your inspection timeline helps us prioritize support.

0/1000

Review & Submit

Please review your application before submitting.

Company Information

Primary Contact

Current Environment

Compliance Priorities

This is well structured for a B2B application. It asks only for information that helps qualify a potential design partner while keeping the application concise and low-friction.

Read-only Deployment

No system access
or data migration

Mutual NDA

Before documentation
review begins

No System Changes

Works within your
existing environment

Human Accountability

Every finding remains
subject to human review

Suricat is building the leading Compliance Intelligence platform for medical device manufacturers.
Your partnership helps build it right.

Application Submitted

Thank you for your interest. Our team will review your application and contact you within 1 business day regarding the next steps.

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