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Clinical Research Translation

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Specialist Clinical Documentation

We provide document-specific translation support for protocols, ICFs, ethics submissions and investigator-facing materials.

Terminology Consistency

We maintain consistent clinical and medical terminology across the project to protect multilingual document integrity.

Controlled Project Workflow

We define scope, confidentiality, quality-control and delivery requirements at the outset.

Reliable Language Support for Clinical Research Teams

Clinical research translation requires protocols, informed consent forms (ICFs), patient information materials and ethics documentation to be handled not only for linguistic accuracy, but also for intended use, audience, terminology and version integrity.

Dilde manages translation and linguistic review workflows for protocols, ICFs, investigator’s brochures, ethics and submission documents, study reports, patient-facing materials and medical correspondence for CROs, sponsors, clinical research teams, regulatory functions and research sites.

We manage terminology, confidentiality, quality control and delivery planning in a single workflow, giving your team consistent, ready-to-use multilingual documentation with less coordination.
Klinik araştırma belgeleri ve temel klinik dokümanlar
PROTOCOLS AND ICFS
Core Clinical Documents

Study protocols, ICFs, patient information and informed consent materials are translated in language that is clear to the intended audience and consistent with the source.

ETHICS AND REGULATORY
Submission Documentation

Documents used for ethics committee, authority and research-site submissions are translated with terminology, version and document integrity preserved.

Terminoloji ve anlam kontrolü süreci
QUALITY CONTROL
Terminology and Meaning Review

We prepare translations for delivery through separate checks for terminology, meaning, spelling, numbers, dates and formatting.

PROJECT MANAGEMENT
Scope and Delivery Planning

We confirm language pairs, file structure, quality requirements and delivery schedule before work begins.

Request a Scope Review and Quote for Your Clinical Research Files

Share your document types, language pairs, approximate word volume, reference terminology and target delivery date. We will review your files and define the project scope, workflow and quotation.
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