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Professional Medical Record translation services in Vietnam

Enabling foreign doctors to provide reliable remote diagnoses and treatment advice, we effectively support medical tourism and global patient care.

End-to-end language support for Patients, families, hospitals/clinics, insurers, law firms, embassies, and relocation/immigration agencies needing accurate Vietnamese ↔ English (and multi-language) translations of personal medical documents.

Clinical trial document types we translate

  • Clinical summaries: discharge notes, history & physicals, operative reports, progress notes

  • Diagnostics: lab results, imaging reports (X-ray/CT/MRI/US), pathology/cytology

  • Prescriptions & treatment plans: medication lists, vaccination cards, immunization records

  • Certificates & forms: medical certificates/fit-to-fly/fit-to-work, sick-leave notes, insurance claim forms, referral letters

  • Specialties: dental charts, obstetric records, pediatric growth charts, mental-health notes, rehabilitation logs

  • Administrative: hospital bills/invoices, receipts, appointment confirmations, consent forms

Our clinical translation quality workflow (TEP/LQA)

Medical Devices Translation In Vietnam
Professional Medical Record Translation Services in Vietnam

Compliance & risk controls in our clinical trial translation services

  • ISO-aligned TEP workflow (Translation–Editing–Proofreading) with medical-domain linguists

  • Plain-language rendering for non-technical recipients while preserving clinical meaning and units

  • PHI handling with least-privilege access; encrypted transfer & storage; NDA on request

  • Redaction on request for sharing with third parties

Certification & legalization

  • Certified translations with translator affidavit and company stamp (per page list of documents)

  • Notarization in Vietnam available

  • Consular legalization/Apostille support as applicable to the destination authority (we align to specific filing instructions).

Note: Acceptance requirements vary by institution; share their instructions and we’ll conform formatting, seals, and signatures accordingly.

Data protection & security

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FAQs

What we need to start a clinical trial translation project?
  • Final or near-final source files (plus tracked-changes version if available)

  • Any prior approvals, glossaries, style guides, IRB/IEC feedback

  • Required deliverable formats (DOCX/PDF/INDD) and template branding

  • Whether back-translation or certified translations are required

Clinical trial translation output
  • Editable bilingual files + clean targets

  • Change log / query log

  • Certificate of Accuracy upon request

Other optional add-ons in clinical trial support
  • In-market linguistic validation for PROs (cognitive debriefing coordination)

  • On-site/virtual interpreter support for investigator meetings and trainings

  • Continuous localization for eCOA/EDC strings (TM-backed)

DTP & format care
  • Print- and submission-ready files (Word, PowerPoint, Excel, IDML/INDD, PDF forms, XLIFF, JSON/RESX, HTML).

  • Layout engineering for right-to-left scripts and double-byte fonts; line-break control, pagination, tables, forms, signature blocks.

Timelines
  • Short patient leaflets (2–6 pages): 24–48h.

  • Protocol/IB chapters: scheduled by wordcount & review cycles.

  • Rush & weekend coverage available.

What an SME LQA deliverable includes
  • Marked-up file (Tracked Changes), Issue Log with severity/rationale, Scorecard, Change glossary, final clean file, and recommendations (e.g., style/guideline updates).