OUR SERVICES

Pharmaceutical Translation Services

Ensure precision and compliance across every phase of the pharmaceutical lifecycle.

Elmura provides certified, human-translated pharmaceutical content in over 200 languages – from clinical trial materials and regulatory documents to packaging and patient information. We ensure clarity, accuracy, and consistency for pharmaceutical organizations working across borders.

Trusted for global communication in life sciences, drug development, and clinical research.

Get a Certified Translation Now

Booking our services is simple:

Submit a contact form with your project requirements, and a team member will follow up during business hours.

Full Name

Language Pair

Details of the Request

Drag & Drop Files, Choose Files to Upload

For interpretation services

Date / Time
*If in-person interpretation is required.

Additional Information

*Special instructions or requirements
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Why Pharmaceutical Companies Choose Elmura

Elmura delivers accurate, compliant, and secure pharmaceutical translations at scale – without AI, shortcuts, or automated guesswork.

✔️ 100% human translation by domain-experienced linguists
✔️ Certified documents ready for regulatory and legal use
✔️ Fast, reliable delivery with optional rush service
✔️ Language support for all major pharmaceutical markets
✔️ Secure file handling and NDA-bound linguists

Whether you’re translating for patient communication or global submissions, we provide reliability without compromise.

Why Pharmaceutical Companies Choose Elmura
Documents We Translate

Translation for Manufacturing & Packaging

Elmura handles technical translation needs across the manufacturing and packaging cycle – from quality control to end-user delivery.

Standard Operating Procedures (SOPs)

Master batch records

Packaging inserts

Labels and barcode instructions

Quality control forms

Documents We Translate

We cover all document types across the drug development and commercialization cycle

Clinical Research Regulatory Patient-Facing Manufacturing
Informed Consent Forms (ICFs) Drug Dossiers Patient Leaflets Batch Records
Case Report Forms (CRFs) Pharmacovigilance Reports Instructions for Use (IFUs) SOPs
Investigator Brochures Product Labels Discharge Instructions Quality Control Docs
Study Protocols Marketing Literature Medication Inserts Packaging Inserts

Have a document type not listed? Let us know – we handle specialized requests.

Pharmaceutical Marketing Translation

We translate pharmaceutical marketing content with a focus on brand consistency and regulatory alignment.

We support localization for regional dialects and ensure that tone, terminology, and formatting meet industry expectations. 

Our team handles a range of materials including product brochures, email campaigns, awareness content, internal training documents, and educational resources for healthcare professionals.

Who We Support

We serve clients globally across various pharmaceutical-adjacent sectors:

Biotech startups

CROs (Clinical Research Organizations)

Medical labs

Pharma marketing teams

International regulatory partners

Drug manufacturing firms

Our translators ensure that tone, sentiment, and context are preserved – making your UGC a powerful conversion tool worldwide.

Translation Accuracy You Can Trust

Elmura’s pharmaceutical translations are handled exclusively by native-speaking linguists with relevant medical and industry experience.

Each document is reviewed through a multi-step human QA process to ensure accuracy and clarity. 

We guarantee consistent use of terminology across all files, adherence to clinical and regulatory language, and proper formatting that maintains readability.

No content is generated through machine translation or unverified AI. Every word is handled by trained professionals.

Clinical Trial Translation Services

We specialize in translating critical documents that support global clinical research

Our clinical trial translation scope includes:

Patient recruitment materials

Informed Consent Forms (ICFs)

Case Report Forms (CRFs)

Investigator brochures

Study protocols

Patient diaries and logs

You’ll receive real-time status updates throughout the process

Certified Translation & Compliance

All pharmaceutical translations come with signed certification of accuracy, formatted for regulatory use.

While we have not yet submitted to FDA or EMA directly, our documentation meets the standards for:

  • Clinical trial documentation
  • International submissions
  • Internal audits
  • Legal recordkeeping

 

Certification includes:
✔ Signed statement of accuracy
✔ Source and target language details
✔ Elmura letterhead and stamp
✔ Optional notarization upon request

Elmura Certifications

Frequently Asked Questions (FAQs)

What file formats do you accept for pharmaceutical translation?

We accept Word, PDF, Excel, PowerPoint, and scanned documents. For structured data files or DTP formats, contact us for review

Yes. We provide support for multi-document, large-scale projects and recurring pharmaceutical translation work.

No. We accept everything from single-page documents to multi-thousand-word technical files.

Yes. Our translators are trained to maintain branding consistency while adhering to regulatory guidelines.

We rely on trained human linguists, multi-step internal QA, and revision cycles to deliver unmatched accuracy without automated shortcuts.

Yes. Upon request, we can show a redacted sample for review to demonstrate our formatting and certification standards.