GHMAP
MHRA market-access overview for class iib devices. Planning intelligence only — not a regulatory determination, approval, or clinical decision support.
Planning ranges for this country and device class. Label every figure as illustrative until sources are verified.
| Metric | Value | Status |
|---|---|---|
| Authority | Medicines and Healthcare products Regulatory Agency (MHRA) | Source tracked |
| Device class | Class IIb | Example only |
| Average timeline | ~240 days / ~8 months (illustrative) | To be verified |
| Local representative required | Yes — UK Responsible Person (UKRP) | To be verified |
| Government / assessment fee | ~$12,000 USD (illustrative) | Source required |
Step-by-step planning outline. Owners and sequence vary by product evidence and authority questions.
Map Class IIb and whether UKCA, CE recognition windows, or other routes apply.
Owner: Manufacturer
UKRP holds regulatory obligations for non-UK manufacturers.
Owner: Manufacturer
UK-aligned technical file, labeling, and QMS evidence.
Owner: Manufacturer
Complete required assessment and MHRA registration.
Owner: Manufacturer / UKRP
Vigilance reporting and continued UKRP oversight.
Owner: UKRP / Manufacturer
Cross-links between pathway pages, country intelligence, and certification primers.
Broader market, reimbursement, and procurement context for United Kingdom.
Open country profilePublic pathway pages are general context. Product-specific decisions use request-first market entry packages with written scope lock before research begins.
$5,000 · 15 business days after complete intake and scope lock
Product-specific market-entry decision for one healthcare or MedTech product in one target country. Includes the Decision Report, Evidence & Calculations Workbook, a 60-minute analyst debrief, and one consolidated revision round.
$7,500 · 20 business days after complete intake and scope lock
Evidence-based distributor search for one defined MedTech or IVD product in one selected country: 10–15 screened candidates, 10 detailed assessments, and 3–5 recommended for outreach when evidence supports it.
Prefer a shorter briefing first? Request a Regulatory Pathway Brief ($1,800).
Market entry packages
GHMAP confirms written scope before Country Intelligence or Distributor Search research begins. Payment never auto-approves introductions or workspace access.
Professional review remains part of every GHMAP deliverable.
