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Medical Devices · 3 months

EU MDR Technical File & CER Multilingual Program

Translated MDR technical files, clinical evaluation reports and PMCF plans for a Class IIb device with notified body review.

3
Languages
2200+
Pages
3
Months
0
Translation NB findings

背景

A client migrating CE certification to MDR needed upgraded MDD materials in EN/DE—GSPR mapping, risk management, clinical evaluation and post-market surveillance files.

成果

Zero translation-related findings in NB first-round queries; supplements submitted on time

サービス内容:

MDR tech filesCER translationPMCF docs

対応言語:

ChineseEnglishGerman
関連業界を見る: MDR Translation

プロジェクトの課題

MDR requirements

Accurate GSPR and PMCF language.

Large CER

Literature citations and data tables formatted consistently.

NB tone

Language aligned with notified body expectations.

Cross-references

Section numbering and reference chains intact.

アプローチ

品質、コンプライアンス、納期のバランスを取った段階的納品。

01

Regulatory alignment

Confirm target markets, doc types and authority expectations.

02

Medical glossary

IFU/label/clinical glossary and do-not-translate lists.

03

Med TEP + DTP

Medical linguists, second review and layout fidelity.

04

Submission packaging

Organized deliverables per filing templates and change logs.

成果物

Technical file CER PMCF plan GSPR checklist

Project highlights

📋

MDR migration

MDD→MDR structure upgrade support.

🔬

CER expertise

Clinical data and citation accuracy.

🇩🇪

German NB

German notified body phrasing.

🔗

Cross-refs

Full reference chain QA.

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