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Help Define the Future of
Compliance Intelligence.

Join a select group of medical device manufacturers collaborating directly with the Suricat founding team to shape the future of Compliance Intelligence.

Limited to a small cohort of medical device manufacturers.
5-minute application
Response within 3 business days
No obligation
The Program

A focused engagement built to validate measurable outcomes.

Collaborate directly with Suricat's founders to validate findings, gather feedback, and determine mutual fit with minimal disruption to your team.

Founding Cohort

Be among the first 5-10 medical device manufacturers helping define the future of Compliance Intelligence.

Your feedback will directly shape the Suricat platform before general availability.

Only 5-10 organizations in this inaugural cohort.

What You'll Receive

  • Executive findings summary
  • Evidence mapping report
  • Potential documentation misalignments
  • Inspection readiness observations
  • Recommendations for next steps
  • Direct influence on the product roadmap
  • Preferred consideration for early adoption
Actionable outputs you can use immediately.

What We'll Ask

  • Executive Sponsor

    Provides alignment and strategic oversight

  • Representative Documentation

    Share key documents to enable meaningful analysis

  • Weekly Collaboration Sessions

    ~2-3 hours per week with our founding team

  • Subject Matter Expertise

    Input from your team as needed

  • Founder Collaboration

    Work directly with Suricat founding team throughout the engagement

  • Approximately 2-3 hours per week.

Typical Time Commitment

Executive Sponsor

~1hr / week

QA / RA Lead

~2-3 hrs / week

Subject Matter Experts

As needed

Total Organizational Investment

20–30 Hours

Across 30 Days

Ideal Partners

Who should apply?

We're looking for forward-thinking medical device manufacturers that are committed to raising the bar for quality and compliance.

Medical Device Manufacturers

Building safe, effective products for patients worldwide.

ISO 13485 Certified

Operating under ISO 13485 or preparing for certification.

Preparing for FDA Inspection

Seeking greater confidence and readiness for regulatory inspections.

Complex Quality Environment

Managing multiple systems, interconnected processes, and documentation.

Also ideal for organizations with multiple documentation systems and increasing regulatory complexity.

Frequently Asked Questions

No. Suricat operates as a read-only Compliance Intelligence Layer above your existing quality and documentation systems. There is no rip-and-replace, data migration, or disruption to your validated environment.

Yes. A mutual NDA is executed before any documentation is reviewed. Protecting your confidential information is a foundational part of the Design Partner program.

We typically review a representative set of quality and regulatory documentation, which may include SOPs, work instructions, risk management files, CAPAs, design documentation, and supporting records. The exact scope is determined collaboratively based on your environment and objectives.

The program is most effective when supported by a small cross-functional team, typically including a Quality or Regulatory leader, an executive sponsor, and subject matter experts as needed throughout the engagement.

Most Design Partners invest approximately 20–30 hours over a 30-day engagement, with an average of 2–3 hours per week for collaboration sessions, document reviews, and feedback.

At the conclusion of the engagement, you'll receive an executive findings summary, documentation alignment insights, and recommendations. Together, we'll review the results, gather your feedback, and discuss next steps, including potential continued collaboration.

No. There is no fee to participate in the Design Partner program. Participation is based on mutual fit, collaboration, and a willingness to provide feedback that helps shape the platform.

Your documentation remains your property. Suricat reviews approved materials under a mutual NDA, operates in a read-only manner, and never modifies your validated systems. Every finding is supported by traceable evidence and remains subject to human review.

No. Your documentation is never used to train foundation models or shared with other customers. Your information remains confidential and is used only to support your Design Partner engagement unless you explicitly authorize otherwise.

Become One of Suricat's Founding Design Partners.

Join a small group of industry leaders driving the next generation of Compliance Intelligence—together with Suricat.

Enterprise-grade security

Your data stays in your environment.

Confidential engagement

Your information is always protected.

Founder-led experience

Work directly with our leadership.