Start Your LatAm Pilot

Amavita Sciences™ helps foreign medtech and biopharma companies run clinical trials and secure regulatory approvals across Latin America — faster, and with translational-services readiness for regulators in Argentina, Brazil, Mexico, and beyond. Tell us about your program below and our team will reach out within 2 business days.

Pilot Intake

Tell us what you are trying to launch in Latin America.

Share the countries, product type, and timing. Your request is sent directly to the Amavita team.

Quote request

Requesting a quote for: Tier 1-B — Standard regulatory translation ($0.19–0.24/word)

We prefilled your program details with the selected tier. Edit any field below before sending.

Name

Work email

Company

Role

Target countries

Program type

Timeline

Program details

Prefer email? Write to hello@amavitasciences.com. Our team will reach out within 2 business days.

Before you submit

How Amavita handles regulatory translation.

Preview the workflow, coverage, and regulator-specific requirements before your team fills out the pilot brief.

Clinical Trial Translation Services

Hub for LatAm regulator coverage, MD-led review, and the First-Pass Acceptance SLA.

ANVISA requirements (Brazil)

Portuguese submission rules, tradutor público juramentado, and common exigências.

COFEPRIS requirements (Mexico)

Spanish submission rules for COFEPRIS clinical trials and registrations.

LatAm market access impact

How translation quality shapes the speed of market clearance and audit success.