Advisory for:Health Tech Scale-Ups

Manage growing regulatory obligations, new procurement targets, and product updates without building expensive in-house compliance capability.

The Challenge

Where scale-ups get stretched

Scaling a digital health product introduces compliance complexity that early-stage documentation was never built to handle. New features change your clinical risk profile. New markets introduce new regulatory obligations. New procurement targets require evidence standards your existing documentation does not meet.

Most scale-up compliance teams are stretched thin — maintaining what exists while trying to build what is needed next.

Safety case and hazard log not updated for new product releases
Fragmented reporting and delayed insights
No CSO capacity to manage growing compliance workload
Investor due diligence exposing regulatory documentation gaps
International expansion creating new regulatory obligations

Our Deliverables

What we help scale-ups with

Efficiency
Documentation Management

Keeping your compliance documentation current as your product grows.

Operations
Expansion Readiness

Building the evidence stack for new markets and procurement targets.

Future Readiness
Governance Infrastructure

Building compliance infrastructure that scales with the business.

See what's possible

SCALE-UP
UPDATE
Post-Release Safety Case Update
INPUTS
Major product release requiring safety case revision
AUTO
Review
New Hazards
Update Log
Re-certify
RESULT
SCALE-UP
FRAMEWORK
NHS Framework Application
INPUTS
Product seeking placement on NHS procurement framework
AUTO
Requirements Map
Evidence Pack
Submission
RESULT
SCALE-UP
DUE DILIGENCE
Investor Due Diligence Support
INPUTS
Investor requesting regulatory position documentation
AUTO
Audit
Gap Fix
Position Statement
Investor Pack
RESULT

Typical outcomes

The impact of compliance infrastructure that scales

~50%

reduction in

compliance

management overhead when CSO retainer replaces in-house build

~65%

faster

response

to investor due diligence requests when regulatory documentation is maintained continuously

“Scale-ups that treat compliance as infrastructure rather than a project are the ones that convert the procurement opportunities their competitors miss.”

Dr Jide Idowu, Founder, SDHA

Post-release clinical safety case update for a telemonitoring platform following a significant feature release. Hazard log updated, new risks assessed, and CSO sign-off secured within four weeks.

NHS framework application support for a mental health digital tool. Full evidence pack compiled and submission managed end to end. Product listed on framework within the application window.

Regulatory due diligence package produced for a Series A raise. Investor-ready regulatory position statement, gap-closure roadmap, and MHRA pathway documentation delivered in three weeks.

Connect with an Expert

Let's map your compliance pathway

Tell us about your product and where you are in the process. We will identify your obligations and recommend the right next step.