Clinical trial documents, patient materials, regulatory submissions, and pharmaceutical dossiers translated by Portuguese-speaking medical specialists.
Brazil is Latin America's largest pharmaceutical market and home to ANVISA, the national health surveillance authority with detailed submission requirements. Portugal operates under EMA frameworks. Our Portuguese medical translators are native speakers with medical or pharmaceutical qualifications and experience with both regulatory environments.
Translators with experience in Brazilian ANVISA submissions and Portuguese EMA/INFARMED regulatory documentation.
All Portuguese medical translations handled by translators holding degrees in medicine, pharmacy, or life sciences.
Translation, specialized medical editing, and final terminology review using validated Portuguese medical glossaries.
Patient documents and regulatory materials matched to the correct Portuguese variant for the target market.
“I recently used the BeTranslated France translation service and the experience was absolutely remarkable. The translators were competent, professional and extremely responsive. They were able to understand my specific needs and delivered high quality work on time. I highly recommend this service to anyone who needs accurate and efficient translations. A big thank you to the whole team!”
Google review (FR) , 2 years ago
“They offer great and reasonable prices for sworn translations. Thank you for your help in translating my documents for my legal process.”
Google review (SL) , 6 months ago
“Highly professional and meticulous work. They truly listened to my needs and communicated very responsively. Very satisfied with the work done.”
Google review (FR) , 2 months ago
Yes. Our Brazilian Portuguese medical translators are familiar with ANVISA technical documentation requirements and the specific formatting conventions for drug registration dossiers.
Yes. We can produce two parallel versions in the same project, one in European Portuguese and one in Brazilian Portuguese, with consistent medical terminology throughout.
We create a project-specific glossary and enforce it consistently using CAT tools and translation memories across all documents in the dossier.
In addition to ANVISA (Brazil) and INFARMED (Portugal), we work with Angola's ARMED (Agencia Reguladora de Medicamentos e Tecnologias de Saude), Mozambique's DNAM (Direccao Nacional de Assistencia Medica) regulatory submissions, and Cape Verde's health authority filings. For multi-country Lusophone Africa submissions we run a single source pass and adapt terminology to each national authority's conventions in parallel.
Every translator and project manager signs a GDPR-aligned data processing agreement before receiving any patient-identifiable or trial-confidential material. Files are transferred over encrypted channels, processed on secure infrastructure, and purged from our systems on project closure unless you request translation memory retention. For Brazil-originating projects we apply LGPD (Lei Geral de Protecao de Dados) aligned data handling on top of EU GDPR standard protocols.
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Send us your portuguese medical translation files, language pairs, and deadline. We will confirm specialist availability, certification needs, and a clear quote as quickly as possible.
