The 5 most entry-ready markets for medical devices right now
For a Class II device, the fastest routes belong to the markets that let you build on an approval you already hold.
Market readiness rankings, analysis, and autopsies, written for the teams making the call.
For a Class II device, the fastest routes belong to the markets that let you build on an approval you already hold.
Six large markets, each decided by one specific requirement, and usually not the one companies screen for.
The 100 percent Section 232 tariff extended to all companies on 29 September, and Commerce published the architecture that decides who pays nothing.
International reference pricing enters Medicare Part B by final rule, with a later start and a much shorter list of drugs than proposed.
A 100 percent tariff on imported patented medicines is operative for a first group of companies, and applies to everyone else from 29 September.
WHO and the African Medicines Agency signed a framework to drive regulatory reliance across the continent.
An abbreviated assessment route opens for products already approved by one of six named authorities.
NICE's cost-effectiveness range moved for the first time in two decades, and the Secretary of State can now direct it.
A new GB route recognises US, Canadian and Australian approvals. Not European ones.
Under most-favored-nation and reference pricing, the order of entry has become a pricing decision.
Peer review assumed a human made the analytic decisions and could reconstruct them. That assumption no longer holds.
Tax and customs is the sixth dimension of market entry, and the one almost no assessment measures.
External reference pricing is a sequencing constraint, not a fact of life.
The approval you already hold determines which markets open next.
The registration was never in the company's name, and the company only discovered that when it tried to leave.
A price agreed in a small early market travelled, by rule, into every market the company had been saving.
The company optimised for the regulator, then met a second decision maker it had never designed evidence for.
A therapy withdrawn from a market that had done nothing wrong.