amavita

Start Your LatAm Pilot

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.

Continuación en español

Nuestro equipo confirmará su piloto en español y en un plazo de 2 días hábiles. El formulario a continuación está en inglés; puede responder en español o portugués.

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.

Prefilled from your guide

  • Coming from: COFEPRIS translation requirements guide
  • Requirement type: Full technical guide

We added this context to your program details and program type. Edit any field below before sending.

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.