This is a Spanish-language edition of our flagship India market-entry webinar, designed specifically for LATAM exporters. The full slide deck is bilingual; the session is conducted in Spanish with English Q&A optional.
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.
This is a Spanish-language edition of our flagship India market-entry webinar, designed specifically for LATAM exporters. The full slide deck is bilingual; the session is conducted in Spanish with English Q&A optional.
Free to watch in full · slides linked below
Practical, no-fluff takeaways you can act on the same week.
How CDSCO's evolving Risk-Based Classification reshapes import-licence pathways
When you need an Indian Authorized Representative (IAR) and what the IAR is legally responsible for
Pricing, branding and channel strategies that work for the Indian middle market
Operational realities — bonded warehousing, port clearance, post-market surveillance
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.

Ishita leads Taevas' Global Market Entry practice from Bangalore. She has helped 200+ international medical-device, pharma and consumer-health brands navigate Indian Authorized Representative (IAR) workflows, CDSCO licensing and post-market surveillance — and routinely speaks on the same topics for ECRM, ChemLinked, and the Indian Medical Devices Forum.
Connect on LinkedInA 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.

How a competent Indian Authorized Representative shortens a 14-month entry into 4–5. Channel strategy, Nykaa/Amazon onboarding, BIS compliance, ladder pricing, and Instagram-led D2C builds — all condensed into one hour.

A 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.
