Roberta and the São Paulo team unpack ANVISA RDC 751/2022 in plain English, with case studies from medical-device, pharma, and consumer-health brands that have launched in the past 18 months.
Gain insights into the essential steps for successfully entering the Brazil market for medical devices, pharmaceuticals, and consumer products. Learn about the regulatory landscape, the role of a legal representative, and effective strategies to streamline the market entry process.
Roberta and the São Paulo team unpack ANVISA RDC 751/2022 in plain English, with case studies from medical-device, pharma, and consumer-health brands that have launched in the past 18 months.
Free to watch in full · slides linked below
Practical, 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.
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