Evidaxia
Market access

Market access consultancy, from evidence to agreed price.

Access strategy that connects the evidence, the HTA submission, the pricing agreement and uptake in practice, for pharmaceutical, biotech and MedTech companies.

Reviewed by Hasan Bari, Founder and Managing Director · Updated October 2026

Access is decided long before launch

The evidence that determines access is largely fixed by the time a product reaches HTA. Comparators, endpoints, follow-up and subgroups are set in the trial programme years earlier. Market access strategy therefore has to start early, connect clinical development with the questions payers will ask, and keep the value story consistent from the first advisory board to the final pricing agreement.

What we deliver

  • Market access strategy and integrated evidence planning
  • Payer landscaping, stakeholder mapping and value message testing
  • Global value dossiers, value stories and payer question-and-answer guides
  • HTA submissions in the UK, Ireland and the EU
  • Pricing and reimbursement strategy, launch sequencing and international reference pricing and MFN analysis
  • Managed access and commercial arrangement design
  • Adoption and uptake planning, including local business cases

Market access in Ireland

In Ireland, the HSE Corporate Pharmaceutical Unit commissions the NCPE, every medicine starts with a rapid review, and the CPU leads the commercial negotiation. Market access consultancy in Ireland therefore means planning the rapid review, the possible full HTA and the commercial offer as one piece of work, with budget impact in view from day one. See NCPE submissions and HSE reimbursement.

Market access in the UK

In the UK, access runs through NICE in England, the SMC in Scotland and AWMSG in Wales, each with its own process and timelines. NICE has used a range of £25,000 to £35,000 per QALY since April 2026, and managed access can bridge evidence gaps for promising medicines. See NICE, SMC and AWMSG submissions, SMC submissions and managed access.

Market access across Europe

Across the EU, the joint clinical assessment now feeds national decisions on value and price in each Member State. Our HTA requirements comparison sets the main systems side by side, with detailed pages for Germany, France, the Netherlands, Belgium, the Nordics and Romania. US pricing interacts through MFN: see our analysis of MFN and European launches.

Why Evidaxia

We bring HTA assessor experience, health economic depth and senior strategic judgement to the same table, so access strategy is grounded in what the evidence can actually support.

Pricing strategy
“The pricing analysis helped us decide where to focus and what to expect from international reference pricing. It gave the team a clear view of the trade-offs rather than a long list of options.”
Head of Pricing and Access, biotech company

Client names are withheld at their request for confidentiality.

FAQ

Common questions

Anything else? Email info@evidaxia.com.

What does a market access consultancy do?

It helps life sciences companies secure reimbursement and uptake by aligning evidence generation, HTA submissions, pricing strategy and value communication with what payers and health systems need.

Do you work on MedTech as well as medicines?

Yes, including NICE HealthTech guidance, diagnostics and devices, as well as medicines and advanced therapies.

How does US MFN pricing affect European access strategy?

Because US benchmarks can reference European prices, launch sequencing and price levels in the UK, Ireland and the EU now interact with US revenue. We model those interactions.

Do you provide market access consultancy in Ireland?

Yes. We support NCPE rapid review and full HTA submissions, resubmissions, budget impact analysis and the commercial offer to the HSE, as one access plan.

Do you provide market access consultancy in the UK?

Yes. We support NICE, SMC and AWMSG submissions, managed access and commercial arrangements, led by a former NICE HTA Technical Lead and Analyst.

When should market access work begin?

During clinical development, ideally before pivotal trial design is fixed, so the evidence answers the questions HTA bodies and payers will ask.

Start a conversation

Talk to a senior consultant about your submission.

Start with a free, no-obligation 30-minute call with a senior consultant.