Professional & Certified Pharmaceutical Translation Services

Looking for reliable pharmaceutical translation support? You’re in the right place. Transcription Services US offers professional & certified pharmaceutical translation services that cover everything from technical documents to chemical data—no detail is too small. Our translators don’t just know languages—they understand the pharmaceutical industry inside and out, making it easier to translate complex medical terms and corporate materials accurately into the language you need. Our prices start at $0.10/word for document translation and $7/minute for audio translation. Dial US:1-800-230-7918. for more details.

We believe that accuracy in this field can’t be left to chance, which is why we only provide manual pharmaceutical translation. No automated tools or shortcuts—just experienced professionals who take every word seriously. Whether it’s a product document or a press release, our team knows how crucial it is to get every detail right.

A translators is providing certified pharmaceutical for a client, ensuring regulatory compliance and document accuracy.

There’s simply no room for mistakes when it comes to pharmaceutical labeling, patient leaflets, or technical data sheets. These materials are vital to both safety and compliance, and we treat them with the care they deserve.


A translator manually handles pharma-translation, ensuring technical data and formatting precisely retained for compliance.

Accurate and Manual Pharmaceutical Translation Services

Over the years, we’ve worked with clients across the globe and this has sharpened our skills in pharmaceutical translation and localization services. We tailor every project to meet cultural, regulatory, and industry-specific standards.

For clients who need precision in one of Europe’s most significant languages, we also provide expert German translation services. Our translators combine in-depth knowledge of the source and target languages with a strong grasp of medical terminology. We don’t just translate word-for-word; we understand context, ensuring every translation is accurate, natural, and ready for global use.

This thoughtful and human approach helps us deliver fast, high-quality results—and it’s one of the reasons why we’re a trusted name in professional pharmaceutical translation. Regulatory bodies such as the FDA and EMA require submissions to be in specific formats like eCTD (Electronic Common Technical Document), where layout errors can delay approvals. We ensure formatting and layout retention for every document, maintain glossary and terminology consistency throughout the translation.

Comprehensive Pharmaceutical Document Translation Services

Transcription Services US offers medical translation services for a wide range of pharmaceutical documents, including:

• Clinical trial protocols and reports

✓ Informed consent forms (ICFs)

✓ Patient information leaflets

Research manuscripts and scientific publications

✓ Patient-Reported Outcome (PRO) documentation

✓ Regulatory submissions (e.g., FDA, EMA)

✓ Registration documentation

✓ Patents

✓ Standard Operating Procedures (SOPs)

✓ Quality assurance documentation

Technical data sheets

✓ Equipment manuals and instructions for use

✓ Manufacturing process documents

✓ Drug labeling and packaging text

✓ Advertising and brand promotion materials

✓ Product information brochures

✓ Training documents and records

Media translation services, and much more.

A customers accesses pharmaceutical-translation for diverse pharma documents, including SOPs and quality assurance records.

The global pharmaceutical industry generates thousands of pages of documentation per drug—ranging from clinical trials to labeling and marketing materials. Preparing a new drug application (NDA) for regulatory bodies such as the FDA or EMA can involve compiling of detailed documentation, covering everything from clinical data to manufacturing processes. Our translators are well-trained to handle this level of complexity and ensure accurate, regulation-compliant translations across all document types


A customer is assisted by a certified pharmaceutical-translation professional, benefiting from secure and timely service.

Why Choose Us for Pharmaceutical Translation Services?

When it comes to pharmaceutical translation services, we know how important accuracy, confidentiality, and trust are. Whether you need a single document or your entire pharmaceutical brand website translated, we’re here to help—with attention to detail and a commitment to meeting your deadlines.

We don’t just offer careful medical translation services—we also make sure your information stays private, your deadlines are respected, and your expectations are exceeded. Our experienced pharmaceutical translators bring native-level language skills and deep industry knowledge to every project, no matter how complex.


We proudly deliver high-quality, country-specific pharmaceutical translation and localization services that meet both regulatory requirements and your unique needs.

Ready to get started? Call us today at 1-800-230-7918!

Here’s what makes us a trusted choice for pharmaceutical translation services:

✓ We’re an ISO-certified pharmaceutical translation agency

✓ Our team includes qualified translators with proven experience

✓ We translate into and from 100+ languages

✓ We’ve delivered highly satisfactory results to clients worldwide

✓ Every project is reviewed by skilled editors and proofreaders before delivery

✓ We’re happy to sign an NDA to ensure your confidentiality

✓ We offer secure payment modes for your peace of mind

✓ We provide dedicated project manager support

The International Organization for Standardization (ISO) outlines standards like ISO 17100 and ISO 13485 to ensure quality in medical and pharma translations. These standards are critical for avoiding costly errors. Our pharmaceutical translation services meet these rigorous standards to deliver quality, accuracy, and reliability you can count on.

Industries Served Within Pharmaceuticals

Here is a list of industries we serve within the pharma sector:

• Biotechnology companies

• Contract Research Organizations (CROs)

• Medical device manufacturers

• Clinical trial centers

• Hospitals and healthcare institutions

• Regulatory agencies

• Pharmaceutical marketing firms, etc.

The pharmaceutical supply chain spans over five major verticals—from R&D and clinical trials to manufacturing, packaging, regulatory compliance, and distribution.

A client receives pharmaceutical-translation specific to packaging and distribution within the pharmaceutical industry.

Each has its own terminology and document requirements. We tailor our translations to the specific linguistic and technical demands of each pharmaceutical sector we serve.


A customer relies on region-specific pharmaceutical-translation for regulatory submissions and product labeling.

Trusted by Pharmaceutical Companies Across Regions

We’ve had the privilege of working with a wide range of pharmaceutical companies—everything from growing SMEs to well-known multinational brands. What sets us apart is how closely we listen to your goals and requirements. Instead of offering a standard solution, we focus on providing translation services that are client-specific and built around what matters most to you.

In the pharmaceutical industry, we know there's no room for error and that every document must meet strict industry standards and terminologies. That’s why our industry-specific translation services are designed to handle the fine details and technical language unique to this field.

We also understand that your message needs to connect with audiences in different locations. That’s why we offer specialized support for businesses in Charleston, West Melbourne, and tampa, adapting translations to reflect the tone, culture, and expectations of each local market.

We keep our pricing competitive without ever compromising on quality. Your documents are treated with complete confidentiality, and we’re committed to delivering everything with a fast turnaround time, so you’re never left waiting.

Why Accurate Pharmaceutical Translation Matters?

A value-driven list that addresses client pain points:

✓ Avoids regulatory delays

✓ Ensures patient safety and informed consent

✓ Supports successful clinical trials in global markets

✓ Maintains brand trust and reputation

✓ Complies with legal and ethical standards

According to ClinicalTrials.gov, over 40% of clinical trials are conducted outside the United States, making multilingual documentation essential for global compliance and patient safety. We offer translation in over 100 language pairs to support global reach and ensure nothing gets lost in translation.

A translator ensures patient safety and regulatory compliance through precise pharma-translation of informed consent forms.

Case Study: English to German – Pharmaceutical Translation Services

Client Information

Client Industry: Pharmaceutical

Location: Germany

File Information

File Type & Duration/Page Count: PDF regulatory documents, 58 pages

Goal

The client, a Germany-based pharmaceutical company, sought precise and compliant translation of its clinical trial documentation from English to German. These documents were critical for a new drug application to the European Medicines Agency (EMA). The client emphasized the importance of accuracy, medical terminology consistency, and adherence to EU regulatory language standards. The objective was to ensure full regulatory compliance without compromising scientific clarity.

Key Challenges

  • Complex medical terminology and regulatory jargon
  • Requirement for localization in alignment with EMA guidelines
  • Tight deadline due to an approaching submission window
  • Need for certified translation with back-translation for QA

Speakers & Languages

Languages: English (source), German (target)

Speakers: Not applicable (document-based content)

Delivery Time

Delivered within 3-4 days

Strategy

A team of native German linguists with expertise in medical and regulatory translation was assembled. The workflow included:

  • Terminology extraction and glossary development
  • Dual-phase translation and medical review
  • Back-translation and reconciliation
  • Final QA check by a certified medical proofreader

All content was processed under strict ISO 17100 standards for translation services, and translation memory tools were employed to maintain consistency across technical sections.

Results

  • 100% compliance with EMA submission requirements
  • Reduced internal review time by 40% due to terminology consistency
  • Successful on-time submission of clinical documentation
  • Strengthened the client's confidence in multilingual regulatory processes

Testimonial

"The precision and professionalism exceeded our expectations. This service gave us complete confidence during a crucial phase of our regulatory process."

– Project Manager, Pharmaceutical Industry
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