We help pharmaceutical companies launch every drug in Brazil at the price it is worth, within CMED rules and with no tax surprises.

Where your drug’s market access is decided
What we deliver
You get finished work, with every number traceable to its source. We start as a specialist advisory; the same modules grow into a platform.

Services
Pricing and access strategy from launch through the lifecycle, including the Price Information Document (DIP) ready for CMED.
CMED category classification, Anvisa queue and timeline reading, and CMED, Conitec and ANS precedents.
NCM classification under TIPI, PIS/Cofins and ICMS regimes, and their effect on Factory and Consumer Prices.
Reference-country baskets built from official sources, and launch-sequence analysis across markets.
Evidence and positioning to negotiate with SUS, private health plans and public buyers.
An early read on the evidence a submission will rely on.
How the system funds, assesses and prioritises care: SUS, private health plans and public procurement.
Access and reimbursement pathways planned market by market.
Each market's access environment, to decide where and when to enter.

Why Mindsharp
Data the market does not have, people who know drug price regulation from the inside, and technology in service of judgment.
Marketing authorization, regulated price and the CMED queue cross-referenced product by product in our own data lake, updated with every Official Gazette issue.
Specialists in economic regulation and CMED pricing methodology, with Pedro Bernardo, former Director of Economic Regulation at Interfarma, as associate.
Every price, exchange rate and tax rate traces back to its origin: CMED, Anvisa, Central Bank, TIPI and the Official Gazette.
We teach AI our team's skills. Repetitive work is automated and expert time goes to the decision.
Reference-country prices collected from each country's official sources and converted at the Central Bank PTAX rate.
One team covers all three domains. The tax effect is built into the price from the start, not added later.
Every number has a source. Every recommendation has a rationale.
Contact
Tell us the product, the timeline and the question. We reply with the regulatory path and what the dossier needs.
