ISO 13485 translation SOPs · Records · Audits · Suppliers
Multilingual quality manuals, procedures, work instructions and audit evidence for global sites and NB audits.
ISO 13485 translation services
Documentation across the medtech lifecycle and compliance.
Regulatory dossiers
CTD/eCTD, technical files and DoC with multilingual translation and formatting.
IFU & labeling
IFUs, labels, package inserts and warnings with medical-grade translation and layout.
Clinical & CRO docs
ICF, CRF, CSR and ethics materials with medical TEP and consistency review.
QMS & audit files
SOPs, CAPA, internal audit reports and QMS documentation.
Product types
Devices, IVD and SaMD manufacturers.
Active devices
Monitoring, imaging and therapy devices
Non-active devices
Implants, surgical and consumables
IVD
IVD reagents and instruments
SaMD
Medical software and AI devices
CRO & sponsors
Clinical trials and regulatory outsourcing
Distributors
Import registration and change files
Medtech translation challenges
Complex regulatory paths—translation errors risk rejection or patient harm.
Regulatory variance
MDR/FDA/NMPA requirements differ
Our approach:
Market-specific templates and review checklists
Medical terminology
Clinical and engineering terms must be exact
Our approach:
Medical linguists + second medical reviewer
Labeling & warnings
IFUs and labels must match figures
Our approach:
Figure-alignment QC and DTP fidelity
Confidentiality & audit
Pre-market data is sensitive
Our approach:
NDA, role-based access and audit trails
Reference projects
Typical medtech delivery scenarios.
Class II EU MDR submission pack
IFU and technical file EN/DE/FR for notified body review.
Outcomes
Passed notified body written inquiries
Languages
FDA 510(k) IFU translation
CN IFU to FDA-format English IFU and labeling.
Outcomes
Faster response to FDA supplement requests
Languages
Why Linguist for medtech translation
Medical and regulatory expertise to reduce rejection and safety risk.
Medical linguists
Medtech translators and reviewers
Regulatory paths
MDR/FDA/NMPA dossier structures
IFU expertise
Strict warning and layout alignment
Secure compliance
Medtech data handling standards
Related resources
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Related industry solutions
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Medtech registration, IFU, labeling and clinical docs—medical linguists plus review for MDR/FDA/NMPA compliance.
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Medical device IFU translation with strict warning, illustration and layout alignment for FDA/MDR filings.
- MDR translation
EU MDR 2017/745 technical files, clinical evaluation, PMCF and DoC—aligned with notified body review language.
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