Medical Translation
Medical TranslationManaging 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 TranslationMedical 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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Medical TranslationHow 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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Medical TranslationTranslation 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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Medical TranslationTranslating 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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Medical TranslationTranslating 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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Medical TranslationTranslating 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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Pharmaceutical TranslationMedical 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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Medical TranslationTranslating Medical Records for a Second Opinion Abroad
Certified translation of medical records for second opinions abroad. M21Global provides ISO 17100-certified medical translations. Free quote within 3 business hours.
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Pharmaceutical TranslationMDR User Manual Translation: Requirements and Certified Process
MDR-compliant user manual translation for medical devices. ISO 17100 certified by Bureau Veritas, covering all EU official languages.
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Pharmaceutical TranslationPharmacovigilance Report Translation for INFARMED and the EMA
How to translate PSURs, ICSRs and RMPs for INFARMED and the EMA: regulatory requirements, terminology pitfalls, and quality control process explained.
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Pharmaceutical TranslationMedical Device Documentation Translation for MDR Compliance
Medical device documentation translation for MDR 2017/745 compliance: IFU, SSCP, labelling and technical files with ISO 17100 certification. Request a quote.
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