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Book a complimentary call to get an expert opinion on where you are on your compliance journey.
Build safer health solutions with guidance
from accredited Clinical Safety Officers.
Our CSOs help you design, document, and evidence clinical-risk management across DCB 0129 and more, giving you the confidence that every release is safe and compliant.
• Trusted by the World's Leading Healthtech Innovators •
Clinical safety,
built into how you work.
Clinical safety isn’t just paperwork to be signed off. It’s how you prove your product protects patients from the very first design decision. Our CSOs work with your product, engineering, and regulatory teams to integrate safety into development, align with your QMS, and maintain the evidence regulators expect to see.
- Develop a Clinical-Risk Management Plan aligned to DCB 0129.
- Build and maintain a Hazard Log that captures and controls risks throughout the lifecycle.
- Prepare or review Safety Case Reports for NHS assurance and MDR compliance.
- Advise on change control, incident management, and post-market vigilance.
Bake clinical safety into every stage of your solution’s development.
Led by Accredited Experts
Our CSOs combine frontline clinical experience with regulatory knowledge, guiding you through the structure, language, and expectations of NHS, MDR, and ISO frameworks.
They review your documentation, risk logs, and safety reports to ensure everything aligns with NHS expectations and best practice.
Proactive, Not Reactive
We’ll help your teams build the right policies, processes, and risk controls from the start.
Your CSO provides clear, actionable guidance to ensure your hazards are captured, assessed, and mitigated, keeping you confident at every stage of development.
Confidence for the NHS and Beyond
Our CSO service gives you structured, credible evidence of clinical safety, recognised across DTAC, MDR, and NHS frameworks like DCB 0129.
You’ll have the assurance that your documentation and risk processes meet the standards buyers, auditors, and regulators expect.
Compliance made easy, clients left beaming.
Discover how companies like yours have automated compliance, unlocked new markets, and ditched the compliance chaos.
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The right plan for every stage of your compliance journey.
Start with what you need today and scale to what tomorrow demands.
Join hundreds of digital health innovators simplifying compliance with Squirrel™ 2.0
Starter Plan
£249
Standard Plan
£370
Pro Plan
£970
Starter Plan
£2,499
Standard Plan
£3,996
Pro Plan
£10,476
With every package you have the option to purchase add on services as needed:
You could get compliance assistance from a number of places.
Other compliance consultants
Can guide you through audits and help with one or two frameworks...
But
They’re often costly, hard to scale, and rarely equipped to manage the complexity of healthtech.
Other compliance platforms
Can automate evidence collection and tick-box tasks for traditional frameworks...
But
They don’t cover the full scope of healthcare frameworks or include expert regulatory support.
Reasons Squirrel™ 2.0 is the best of both worlds:
As smart as a consulting company. As affordable as a compliance platform. Better than both.
And we warranty all of your evidence, meaning...
No more compliance delays.
Ditch the paperwork and launch lightning-fast.
Let Squirrel™ 2.0 handle compliance for you, 10x faster. Let’s get on a call, and we’ll show you how.
