Market Access & Pricing Strategy
I work with pre-commercial biotech teams and market access consultancies navigating high-stakes pricing and access decisions (EU JCA, IRP sequencing, HTA governance, and pricing systems) where strategic clarity at the right moment changes outcomes.
What I do
Launch price policy (gross & net floors), IRP cascade modelling, launch sequence optimisation, analogue benchmarking, and international price business cases across 60+ markets.
EU JCA dossier strategy, PICO structuring, comparator strategy, ITC oversight, cost-effectiveness modelling supervision, and submission positioning for NICE, G-BA, HAS, and CDA-AMC.
Design and implementation of global pricing governance frameworks: approval thresholds, escalation pathways, pricing committee structures, and systems integration across NAVLIN and EVERSANA platforms.
Fractional market access and pricing leadership for pre-commercial biotechs: evidence gap analysis, IEP development, Phase II/III trial design implications, and IRA/MFN ex-US net price impact sizing.
One-time payment models, outcomes-based instalment structures, annuity frameworks, and payer-aligned value demonstration for cell and gene therapy assets navigating complex reimbursement environments.
"10 years across AbbVie, Allergan, and leading market access consultancies including IQVIA, IHS Markit, and EVERSANA. Pricing governance frameworks built and adopted across 60+ markets. Executive-level presentations to SVP and C-suite. EU JCA strategy from Phase II through submission. Japan (PMDA) and China (NMPA) market access experience. PharmD and MPH trained, with advanced HTA and pricing methodology qualifications from Sheffield, Johns Hopkins, and Erasmus."
Moez Katet, Founder · Based in London, UK · Available for engagements across UK, EU, US, Japan, China, and international marketsWho I work with
Many US biotechs with strong domestic commercial positions lack the in-house expertise to navigate EU and international market access. I build the OUS market access and pricing foundation (EU JCA readiness, IRP strategy, HTA positioning) so that ex-US launch doesn't erode the US price or delay access.
Phase II/III biotechs preparing for their first major launch often lack in-house HTA and pricing expertise at the exact moment they need it most. I step in as a fractional Global Market Access & Pricing Director to build the strategy, challenge assumptions, and bulletproof the commercial case before out-licensing or approval.
Boutique market access agencies frequently win large pricing and HTA mandates that require more senior bandwidth than their team can absorb. I work as an embedded senior partner, handling the strategic market access and pricing portions of client briefs with director-level quality and full discretion.
How I engage
A 45-minute scoping call, no commitment required. You explain the challenge, I tell you honestly whether and how I can help.
A clear, one-page engagement summary covering scope, deliverables, timeline, and fees. No ambiguity.
Work begins. Structured updates throughout. Direct access to me at every stage.
Contact
Whether you're a biotech building your first global pricing strategy or a consultancy looking for a senior subcontract partner, I'm happy to start with a conversation.
Engagements typically begin with a no-commitment scoping call.