Roberta and the Brazil team distil 18 months of post-RDC 751 launches into a single hour. Includes case-study walkthroughs and a printable rejection-reason cheat sheet.
A São Paulo-led briefing on what it actually takes to launch and price a pharmaceutical product in Brazil today — ANVISA dossier expectations, CMED pricing pathways, post-launch SUS dynamics, and the most common rejection reasons in 2026.
Roberta and the Brazil team distil 18 months of post-RDC 751 launches into a single hour. Includes case-study walkthroughs and a printable rejection-reason cheat sheet.
Recording shared with all registrants 24h after the live session
One-click registration — calendar invites land in your inbox the moment you sign up.
Register nowPractical, no-fluff takeaways you can act on the same week.
ANVISA RDC 751/2022 risk classes and which apply to your portfolio
How a Brazilian legal representative differs from a distributor — and why you need both
Customs realities for medical, pharma, and consumer-health imports into Brazil
Cost and timeline benchmarks for fresh-registration vs grandfathering
Tight, well-rehearsed, and always ends on time.
Introductions, attendee map, audio check.
Snapshot of growth drivers, recent regulatory shifts, and what changed in the past 12 months.
Live walk-through of the documents, dossiers, and decision points an entering brand will face.
Vigilance, renewals, port clearance, recall procedures, change-control.
Open-floor questions answered by the speaker.
How to book a 1:1 follow-up consultation and access the slide deck.

Roberta runs Taevas' São Paulo office and is an ANVISA-listed legal representative. She has secured RDC 751/2022 registrations for over 80 international device families and authored Taevas' Brazil cosmetic notification playbook.
Connect on LinkedInA focused 45-minute briefing on the 2026 EU MDR amendments — extended Article 120 transitional periods, the digital UDI pilot, and how Authorised Representative obligations have shifted. Aimed at non-EU brands holding (or seeking) CE marking.

Live workshop walk-through of Mexico's notificación sanitaria pathway for cosmetics and personal-care products. Format requirements, label compliance, and the cost-and-timeline reality of going to market through Sephora MX, Amazon MX, and modern trade.

Conducted in Spanish. Unlock key insights for entering India's market via the Authorized Agent / IAR pathway — regulations, licensing, consumer trends, and the role of an IAR in ensuring compliance. Spanish-language session by special request from the LATAM cohort.
