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Medical Translation

Translating Package Inserts and Pharma Docs for EU RegistrationMedical Translation
Jun 25, 2026

Translating Package Inserts and Pharma Docs for EU Registration

How to translate SmPC, package leaflets and pharma documentation for EU registration: EMA requirements, QRD templates, ISO 17100 quality standards explained.

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Medical Translation: Anatomical, Clinical and Pharmaceutical TermsMedical Translation
Jun 18, 2026

Medical Translation: Anatomical, Clinical and Pharmaceutical Terms

How to evaluate medical translation providers: anatomical, clinical and pharmaceutical terminology, and what separates adequate from insufficient services.

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Certified vs. General Medical Translation: When to Use EachMedical Translation
Jun 11, 2026

Certified vs. General Medical Translation: When to Use Each

Certified or general medical translation? Learn when each type is required, which documents need certification and how to avoid costly compliance errors.

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Pharmaceutical Terminology in PT, ES and FR: A Practical GuideMedical Translation
Jun 04, 2026

Pharmaceutical Terminology in PT, ES and FR: A Practical Guide

Practical glossary of pharmaceutical terminology in Portuguese, Spanish and French. Regulatory, clinical and quality terms for pharmaceutical translation.

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Managing Confidentiality in Clinical Document TranslationMedical Translation
May 28, 2026

Managing Confidentiality in Clinical Document Translation

How to manage confidentiality in clinical document translation: GDPR, DPAs, NDAs, and the operational controls organisations should require from providers.

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Medical Device Export to Angola and Mozambique: Translation RequirementsMedical Translation
May 21, 2026

Medical Device Export to Angola and Mozambique: Translation Requirements

Translation requirements for registering medical devices in Angola and Mozambique: mandatory documents, certification levels, and practical guidance for exporters.

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How to Prepare Clinical Documentation for TranslationMedical Translation
May 14, 2026

How to Prepare Clinical Documentation for Translation

Practical guide for clinical trial sponsors: how to prepare briefings, files, and glossaries for regulatory clinical documentation translation.

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Translation Requirements for MDR Medical Device RegistrationMedical Translation
May 07, 2026

Translation Requirements for MDR Medical Device Registration

MDR 2017/745 translation requirements for medical device registration: IFUs, SSCP, technical documentation and language obligations explained for EU market access.

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Translating Hospital Documentation for JCI Accreditation and ISO 9001Medical Translation
Apr 30, 2026

Translating Hospital Documentation for JCI Accreditation and ISO 9001

Translate hospital documentation for JCI accreditation and ISO 9001 certification. Requirements, document types, and the translation process explained.

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Translating Medico-Legal Expert Reports for Court ProceedingsMedical Translation
Apr 23, 2026

Translating Medico-Legal Expert Reports for Court Proceedings

Certified translation of medico-legal expert reports for court proceedings. Learn document types, certification requirements, and how to ensure admissibility.

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Translating Clinical Research Contracts for International StudiesMedical Translation
Apr 16, 2026

Translating Clinical Research Contracts for International Studies

What clinical research contract translation requires: regulatory obligations, common errors, and ISO 17100 certified process for international clinical studies.

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Medical Device Documentation Translation for EU Registration in 5 CountriesPharmaceutical Translation
Apr 09, 2026

Medical Device Documentation Translation for EU Registration in 5 Countries

ISO 17100-certified translation of medical device technical documentation for EU registration, CE marking and MDR compliance by M21Global.

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