DossierTrans
Hungary Dossier & Technical Document Translation Services
Accurate. EU-Compliant. Authority-Ready.
DossierTrans, a scientific arm of Zoesoe Exports Pvt Ltd, provides end-to-end translation, review, and regulatory query support for Hungary-specific and EU-aligned dossiers and technical documents, fully compliant with Hungarian regulatory authorities and European Union legislation.
We support Hungarian manufacturers, MAHs, importers, distributors, CROs, regulatory consultants, and global companies targeting the Hungarian and EU markets with precise, technically accurate, and authority-acceptable translations, ensuring smooth submissions, approvals, inspections, and lifecycle compliance in Hungary.
Who We Are
DossierTrans is a specialized regulatory translation service provider for the Hungarian and EU market, focused exclusively on scientific, pharmaceutical, medical device, food, and technical documentation.
All translations are performed and reviewed by subject-matter experts, regulatory professionals, and native-language technical reviewers—not general translators.
We ensure that translated dossiers consistently maintain:
• Scientific accuracy
• Regulatory intent
• Terminology consistency
• Compliance with EU / OGYÉI / EMA expectations
Hungary Regulatory Alignment
Our services are fully aligned with the requirements of:
• National Institute of Pharmacy and Nutrition (OGYÉI) – Hungary
• European Medicines Agency (EMA)
• Heads of Medicines Agencies (HMA)
• European Commission – DG SANTE
• EU Clinical Trials Regulation (CTR 536/2014)
• EudraCT / CTIS systems
• Hungarian National Public Health Center (NNK)
• EU Customs & Market Surveillance Authorities
Our Core Services – Hungary
📘 Dossier & Technical Document Translation
• Hungary- and EU-specific CTD / eCTD / non-CTD dossier formats
• Module 1–5 translations for National, MRP, DCP & Centralised procedures
• SmPC, PIL, labeling & artwork text (EU-compliant)
• Hungarian-language patient leaflets & labeling (mandatory)
• Clinical trial documentation (CTD, IB, protocols, ICFs)
• Stability studies, validation & analytical reports
• SOPs, specifications, COAs, SDS & technical files
• Import, manufacturing authorization & GDP/GMP documentation
🔍 Review of Translated Dossiers
• Technical and scientific review of translated documents
• Cross-verification with source dossiers
• Identification of terminology errors, inconsistencies & EU compliance gaps
• Alignment with EMA guidelines, EU GMP/GDP, ICH & Ph. Eur. references
🛡️ Post-Submission Regulatory Query Handling – Hungary
• OGYÉI / EMA questions & deficiency letters related to translated content
• Scientific clarification and EU-style regulatory re-wording support
• Revised translations responding to authority observations
• Coordination with local MAHs, EU regulatory consultants & CROs
Languages We Support (Hungary-Focused)
We provide professional, native-level regulatory translations relevant to Hungarian and EU submissions:
🌍 EU & International Languages
• English
• German
• French
• Spanish
• Italian
• Portuguese
• Russian
🇭🇺 Mandatory & Regional Language Support
• Hungarian – required for labeling, PILs & national submissions
Foreign Language ↔ Hungarian | Foreign Language ↔ English
All translations are reviewed by native Hungarian scientific and regulatory experts experienced with EU procedures.
Industries We Serve – Hungary
We provide specialized translation and review services for:
• Pharmaceuticals & APIs
• Biologics & Biosimilars
• Medical Devices & IVDs
• Clinical Trials & CROs
• OTC & Consumer Health Products
• Food Supplements & Nutraceuticals
• Chemicals & Specialty Materials
Why Choose DossierTrans for Hungary?
✅ EU & Hungary–focused regulatory translation (not generic translation)
✅ Expertise in OGYÉI, EMA, MRP/DCP & Centralised procedures
✅ Native Hungarian scientific & regulatory reviewers
✅ Consistent terminology aligned with EU legislation & Ph. Eur.
✅ Authority-ready multilingual documentation
✅ End-to-end support including post-approval queries & variations
✅ Strict confidentiality & data security
Global & Hungary Regulatory Expertise
Our Hungary services support:
• National and EU marketing authorizations
• Clinical trial submissions via CTIS
• Import & manufacturing authorization dossiers
• Export-support translations for EU & ROW markets
• Post-approval variations, renewals & lifecycle management
Our Commitment
At DossierTrans, we understand that a single mistranslated sentence—especially in Hungarian labeling or PILs—can delay or block an EU or national approval.
That’s why we deliver precision-driven, regulator-acceptable translations, aligned with Hungarian and EU compliance expectations—every time.
DossierTrans – Translating Science into Regulatory Approval in Hungary
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