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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

배경

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.

성과

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

서비스 내용:

MDR tech filesCER translationPMCF docs

지원 언어:

ChineseEnglishGerman
관련 업종 보기: MDR Translation

프로젝트 과제

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.

접근 방법

품질, 컴플라이언스, 일정의 균형을 맞춘 단계별 납품.

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.

납품물

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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