Tell us about your product and where you are in the compliance process. We will review the details and recommend the most practical next step.
Typical projects we work on:
- Building clinical safety cases and hazard logs to DCB0129 standard
- Guiding digital health products through full DTAC submission
- Providing outsourced Clinical Safety Officer cover on retainer
- Supporting NHS and ICB procurement submissions end to end
- Advising international companies on UK digital health market entry
- Mapping MHRA regulatory pathways for SaMD products
During the call we usually:
- Map your current regulatory and compliance position
- Identify the gaps between where you are and procurement-ready
- Outline a realistic timeline and recommended advisory approach
Schedule a discovery call
Tell us about your product and your compliance challenge. We will follow up with the next steps.
After you reach out
What happens next
01
Initial review
We review your product details and the compliance position you have described before the call.
02
Discovery conversation
A focused 45-minute conversation to understand your regulatory obligations, procurement goals, and timeline.
03
Direction
If there is a fit, we outline a recommended advisory approach and next steps — with no obligation to proceed.