Understand the device
Define intended use, target markets, classification, and documentation gaps.
REGULATORY EXPERTISE. REAL-WORLD ACCESS.
Medical innovation.
Meaningful
access.
We help medical device manufacturers navigate regulation and reach new markets. And help people find devices they can trust.
Clinical engineering insight.
Regulatory thinking. Human impact.
THE INTERSECTION OF CARE & COMPLIANCE
Concept imagery · upcoming device range
BUILT FOR THE JOURNEYGlobal innovation.
Local understanding.
Local understanding.
OUR AREAS OF FOCUSNAFDAC pathwaysISO 13485 supportClinical engineeringWest Africa market access
ONE PARTNER. A CLEARER PATH.
Expertise that moves
you forward.
From the first question to the next market, we bring technical knowledge and local context to every step.
Discover all services01
Regulatory affairs
NAFDAC registration
A clearer path from technical dossier to Nigerian market access.
02
Quality systems
ISO 13485 QMS support
Practical quality systems built around your device and your team.
03
Market access
West Africa market entry
Local context. A coordinated strategy. A stronger route to market.
THOUGHTFULLY SOURCED. CLEARLY EXPLAINED.
Everyday support.
A higher standard.
Discover the device range we’re developing, with product documentation and verification at its core.
Explore the upcoming rangeUPCOMING RANGE
Foot & ankle care
Cross-strap ankle support
Sourcing in progress · Enquire for updates
UPCOMING RANGE
Joint & muscle support
Everyday knee sleeve
Sourcing in progress · Enquire for updates
UPCOMING RANGE
Insoles
Heat-moldable insoles
Sourcing in progress · Enquire for updates
Verification comes first. Upcoming concepts are shown for enquiries; sales open only after product details and registration are confirmed.
THE MARKET-ENTRY BLUEPRINT
Complex journey.
Clear next steps.
Build the pathway
Agree the regulatory strategy, local structures, responsibilities, and milestones.
Prepare & submit
Coordinate technical evidence, the dossier, and responses to authority queries.
Enter with confidence
Plan distribution, procurement conversations, and post-registration responsibilities.
Nigeria-first expertise Cameroon partner coordination A plan shaped around your device
VOCLINICAL ENGINEERING
MEETS REGULATORY AFFAIRS
MEETS REGULATORY AFFAIRS
THE PERSON BEHIND THE PATHWAYVincent Olafare
Founder, IIICONSULT GLOBALS LIMITED
EXPERTISE WITH A HUMAN PURPOSE
Better access starts
with understanding.
IIICONSULT was founded on a simple observation: good medical devices do not always reach the people who need them.
Vincent Olafare brings more than six years across device fabrication, hospital biomedical engineering, and health technology consultancy to help bridge that gap.
6+years across the
health technology journey
health technology journey
Oneconnected view of regulation,
clinical needs, and access
clinical needs, and access
A LITTLE CLARITY GOES A LONG WAY
Ideas for a more
informed industry.
MARKET ACCESS · 4 min read
Before your first submission: build a better regulatory brief
Read the articleDEVICE AWARENESS · 3 min read
Five questions to ask before sourcing a medical device
Read the articleQUALITY SYSTEMS · 3 min read
Make quality documentation useful to the people using it
Read the articleYOUR NEXT CHAPTER
Let’s make your
next move a clear one.
From a first regulatory question to a defined market-entry plan, start with a conversation.
Book a consultation