Professional Life Sciences Translation Services | Clinical Trial & Medical Device Documentation

Helping pharmaceutical companies, CROs, biotech innovators, and medical technology leaders communicate with precision, compliance, and cultural accuracy in 120+ languages.

In the fast-moving world of pharmaceuticals and life sciences, the language you use is just as critical as the research you conduct.

A single mistranslation can delay drug approvals, breach regulatory compliance, or compromise patient safety.

PROFESSIONAL EXPERTISE

Industry Challenges & Needs

Pharmaceutical and life sciences companies face unique communication challenges:

  • Strict compliance requirements – Meeting EMA, FDA, MHRA, ICH-GCP, and WHO standards across all documentation.
  • Time-sensitive approvals – Delays in clinical trial or regulatory translations can impact market entry.
  • Patient safety – Every instruction, label, and leaflet must be crystal-clear in every language.
  • Consistency across markets – Product information must be uniform and legally compliant in all regions.
  • Specialised knowledge – Translators must understand scientific and medical terminology.

Services We Offer for Pharma & Life Sciences

We support your operations with a full suite of industry-focused language solutions:

Translation for Pharmaceutical & Life Sciences

Pharmaceutical translation services for clinical trial documents, patient-facing materials, regulatory submissions, packaging, and marketing collateral.

Pharmaceutical Interpretation

Simultaneous and consecutive interpretation for regulatory hearings, investigator meetings, and product launches.

Pharmaceutical Transcription

Accurate transcription of research interviews, clinical trial recordings, and scientific presentations.

Regulatory & Compliance Language Support

Ensuring all translations meet authority-specific requirements (EMA, FDA, MHRA, ICH-GCP).

Localisation for Pharma Software & Training

Adapting e-learning modules, compliance systems, and medical technology interfaces for multilingual teams.

Our Process

Step 1

Consultation & Needs Analysis

We start by understanding your brand, target markets, and project scope to ensure the right approach from day one.

Step 2

Industry-Specialist Translation & Localisation

Your project is handled by translators with proven life sciences experience, adapting content to meet regulatory standards.

Step 3

Quality Assurance

Every project goes through multiple proofreading and editing stages to guarantee accuracy, consistency, and brand alignment.

Step 4

Delivery & Ongoing Support

We meet agreed deadlines and remain available for future updates, regulatory submissions, product launches, or ongoing compliance documentation.

Why Choose LingArch

Faster Turnaround

24–48 hour delivery or same day upon request, with fast-track options available for urgent projects.

Transparency

Flat-rate pricing with real-time status updates. No hidden fees or surprise charges.

Certifications

ISO 9001, EN 15038, GDPR, and ATC-compliant workflows with industry-standard quality systems.

Expertise

20+ years of legal translation experience with proven track record across multiple industries.

Security

Encrypted communication with NDA-bound linguists ensuring complete confidentiality and data protection.

Flexibility

120+ languages supported across all time zones with global coverage and local market expertise.

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LingArch combines expert linguists, industry-specific knowledge, and cutting-edge technology to deliver fast, accurate, and reliable translations tailored to your needs.

ISO 17100 Certified
17+ Years of Experience
1,500+ Accredited Linguistic Partners
Native Legal Experts
GDPR-Compliant Security
Fast Turnaround
Strict Confidentiality
Human Proofreading & AI Tools
ISO 17100 Certified
17+ Years of Experience
1,500+ Accredited Linguistic Partners
Native Legal Experts
GDPR-Compliant Security
Fast Turnaround
Strict Confidentiality
Human Proofreading & AI Tools
Trusted Expertise

Industries we serve

Life Sciences has unique requirements and regulatory standards. We understand the specific terminology, compliance needs, and cultural considerations that matter in life sciences to ensure accurate, compliant translations that protect your business and facilitate global expansion.

Real client success stories

Case Studies

Showcasing our expertise in delivering accurate, culturally-aware translations that protect your business, meet regulatory requirements, and drive global expansion.

Support

Frequently Asked Questions

1: Do you provide certified translations for regulatory submissions?

Yes. Our certified translations are accepted by global health authorities including EMA, FDA, MHRA, and WHO.

2: Can you handle urgent pharma projects?

Absolutely. We have scalable teams and workflows to meet tight drug approval or clinical trial deadlines.

3: Do you offer interpretation for pharmaceutical meetings?

Yes. We provide simultaneous and consecutive interpretation for investigator meetings, regulatory hearings, and product training.

4: How do you ensure accuracy in complex pharmaceutical terminology?

We work with subject matter experts, maintain client-approved glossaries, and follow strict terminology management processes.

5: Can you manage multilingual packaging projects?

Yes. We translate and proofread pharmaceutical labels and inserts to meet local language laws and safety standards.

6: Do you support clinical trial translations in multiple phases?

Yes. We handle documentation for all trial phases, from protocols to results submissions, ensuring ICH-GCP compliance.

7: How do you protect sensitive R&D data?

All files are transferred securely, linguists are bound by NDAs, and workflows meet GDPR and HIPAA standards.

8: Can you localise pharmaceutical training materials?

Yes. We adapt e-learning modules, compliance training, and onboarding materials for global teams.

Get Started

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