Clinical Trial Translation Services for Global Compliance

In clinical trials, precision is non-negotiable. A single mistranslation in regulatory documents or informed consent forms can delay approvals and jeopardize patient safety. That’s why Sawatech delivers accurate, compliant, and accessible clinical trial translation services.

Our services are prompt, securely delivered online, and backed by internationally recognized quality standards. With ISO 9001, ISO 17100, and ISO 18587 certifications, we commit to the highest levels of accuracy and efficiency, helping sponsors and CROs move faster without compromising patient safety or regulatory requirements.

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Clinical Trial Translation Services
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When Translation Errors Put Trials at Risk

In clinical research, every word matters. A single mistake in translation can compromise data integrity, delay approvals, or even put patient safety at risk. The consequences of poor clinical trial translation are costly and far-reaching:

Incorrect patient recruitment

materials damage enrollment rates.

Flawed investigator

brochures risk miscommunication with researchers.

Weak terminology

consistency creates confusion in protocols.

Inaccurate case report

forms lead to invalid data.

Regulatory Submissions Demand More Than Words

Imagine submitting a clinical study only to face costly delays because your regulatory submission translation failed to meet ICH-GCP standards. Or worse, patients withdraw from your trial due to unclear patient recruitment materials. In the life sciences and medical device sectors, translation errors don’t just create confusion—they can lead to compliance violations, regulatory rejections, and loss of trust.

Regulatory Submissions Demand More Than Words

Why Choose Sawatech

With Sawatech, every
campaign is more than just translated —
it’s transformed into messaging that inspires action and
delivers results in every local market.

Marketing Translation Services That Inspire Action Everywhere

At Sawatech, our professional clinical trial translators combine linguistic precision with medical and regulatory expertise.

We adapt your study protocols, informed consent forms (ICFs), case report forms (CRFs), and patient-facing materials to ensure clarity, accuracy, and compliance across global research sites.

By pairing subject-matter expertise with strict ISO 17100 and ICH-GCP–aligned workflows, we safeguard data integrity, protect patient safety, and support regulatory approvals across international clinical trials.

Clinical Translation Services That Inspire Action Everywhere

Clinical Trial Translation Services You Can Rely On

At Sawatech, we bridge the gap between science, regulation, and language. Our clinical trial translation services safeguard compliance, ensure clarity, and support seamless global research.

We help sponsors, CROs, and research sites succeed with:

With Sawatech, your clinical documents—from informed consent forms (ICFs) to
case report forms (CRFs)—are managed by trained experts who understand both science and regulation. We make global trials compliant and accessible.

How Our Clinical Trial Translation Process Works

At Sawatech, every clinical trial project follows a structured, proven workflow to ensure translation accuracy:

Inquiry & Analysis

We first assess documents, project scope, and regulatory requirements.

Team Assignment

Then, we select certified medical translators and subject-matter expert linguists to work on your project.

Translation & Terminology Consistency

Translators apply approved glossaries and terminology management for precision.

Quality Assurance & Compliance Review

Our QA team validates translations against FDA compliance translation, EMA documentation translation, and ICH-GCP translation standards.

Final Delivery & Feedback

Finally, we provide submission-ready files that support global trial management.
How Our Marketing Translation Services Work-02

Trusted Results in Clinical Trial Translation

Sawatech delivers measurable impact by combining medical expertise with linguistic precision.
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These results demonstrate why global life sciences leaders rely on Sawatech to protect patients and accelerate trial success.

FAQs About Our Clinical Trial Translation Services

To help you better understand our approach, here are answers to the most common questions about our services.
Yes, our certified medical translators ensure full regulatory compliance.

Absolutely. We apply strict terminology management protocols.

We cover FDA compliance translation, EMA documentation, and ICH-GCP requirements.

Yes, from informed consent forms to patient recruitment materials.

Through multilingual clinical research solutions and international patient communication support.

What Clients Say About Us

Ready to Get Your Clinical Trial Translations?

Ensure compliance and safeguard patient safety with Sawatech’s expert clinical trial translation services.

Our team delivers accurate, submission-ready translations that accelerate global trial success.

Get a Free Quote