{"id":23657,"date":"2026-09-22T14:29:02","date_gmt":"2026-09-22T11:29:02","guid":{"rendered":"https:\/\/mirora.com\/?page_id=23657"},"modified":"2026-09-28T15:53:43","modified_gmt":"2026-09-28T12:53:43","slug":"klinik-arastirma-cevirisi","status":"publish","type":"page","link":"https:\/\/mirora.com\/en\/clinical-trial-translation\/","title":{"rendered":"Klinik Ara\u015ft\u0131rma \u00c7evirisi"},"content":{"rendered":"
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Medical and Life Sciences<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Clinical Trial Translation<\/span><\/h1>\t\t\t\t<\/div>\n\t\t\t\t
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Clinical trial translation covers every document produced to run a clinical study \u2014 from the protocol that defines how the trial works, to the consent forms participants sign, to the data tools that capture results. A multinational study can generate hundreds of documents, and it is exactly this volume, together with the strict regulatory oversight above it, that sets the field apart from other medical translation. Below you will find what these documents are, which rules govern them and what the translation has to get right.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

\n\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tLet's Discuss Your Project<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Our experience in clinical research<\/div>\t\t\t\t<\/div>\n\t\t
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160+<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Clinical trial over the past three years<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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30+ years<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Medical Translation Expertise<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO 9001<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Certified quality management system<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO 17100<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Consistent Translation Workflow<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Clinical Trial Documentation<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Two document streams<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Clinical trial documents follow two separate paths. Each path has a different reviewer, quality standard, and final version.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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01<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Patient-Related Documents<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Patient-related documents are reviewed by ethics committees and institutional review boards (IRBs). In these documents, clarity and simplicity are paramount. To ensure that participants can understand the study, its risks, and their rights, a language appropriate to the target audience\u2019s reading level is required.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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02<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Documents for Sponsors<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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National regulatory authorities review documents submitted to sponsors. In documents such as the protocol, investigator\u2019s brochure, and clinical trial report, scientific rigor, methodological language, and terminological consistency are of paramount importance.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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In patient-oriented text, clarity and simplicity take precedence, while in sponsor-oriented text, scientific precision is the priority. Treating the two as equivalent leads to shortcomings in one and unnecessary effort in the other.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Our Experience in Numbers<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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More than 160 clinical trials<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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With over thirty years of medical expertise, over the past three years, we have translated the documents for more than 160 clinical trials completely and meticulously.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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30+ years<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Medical specialty<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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160+<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Clinical trial<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO 9001<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Quality Management<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO 17100<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Seamless workflow<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Clinical Trial Documents<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Main types of documents and the characteristics of each<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Documents translated during the clinical trial process vary greatly in terms of their purpose and target audience; each requires a different style and level of validation.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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PROTOKOL \/ IB<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Protocol and investigator\u2019s brochure<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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The protocol is the scientific backbone of the study: objectives, design, inclusion and exclusion criteria, dosing and safety monitoring are all defined here. The investigator\u2019s brochure summarises the product\u2019s clinical and non-clinical data for investigators. Both are dense, sponsor-facing scientific texts, and the translator needs command not only of medical terminology but of the language of statistics and methodology.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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ICF<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Informed consent form (ICF)<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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The consent form allows participants to decide with a full understanding of the study, its risks and their rights. The measure is therefore not accuracy alone but comprehensibility: plain language suited to the reading level of the target audience is expected. Consent forms require ethics committee approval, and on request a back-translation confirms that meaning has been preserved.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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CRF \/ eCRF<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Case report form (CRF) and patient diaries<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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The case report form is the standard record of data collected from each participant and is now mostly used in electronic form (eCRF). Its translation must match the field names in the database exactly; otherwise data entry and analysis become confused. Patient diaries are tools completed by the patients themselves; they must be clear and should pass through linguistic validation.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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CSR<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Clinical study report (CSR)<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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When the study is complete, the results are compiled in the clinical study report and submitted to the authority as part of the marketing authorisation application. The report follows the ICH E3 structure and contains statistical tables, safety data and the interpretation of results; consistency of tables and terminology is decisive in its translation.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Regulatory frameworks<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Regulatory Frameworks in Clinical Trial Translation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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The field sits under several frameworks. In the European Union, the Clinical Trials Regulation (EU CTR \u2014 (EU) 536\/2014) sets the application and documentation requirements; globally, the Good Clinical Practice standard ICH E6(R3) and ICH E8(R1), which lays down general principles for clinical studies, apply.<\/p>

In T\u00fcrkiye, clinical trials are conducted under the oversight of Titck, and patient-facing documents pass through ethics committee approval. Participant-facing documents usually call for clinical expert review and, where needed, back-translation; records of translation versions and translator qualifications are kept as well.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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EU CTR<\/div>\t\t\t\t<\/div>\n\t\t
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(AB) 536\/2014<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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The regulatory framework of the European Union that establishes the application and documentation requirements for clinical trials.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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ICH E6(R3)<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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The Good Clinical Practice (GCP) standard for clinical trials .<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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A framework that regulates the general principles of clinical trials; .<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Clinical study report (CSR)<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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The basic ICH guideline used in the structure of clinical trial reports.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Quality and linguistic validation<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Quality control process for regulated documents<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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In a regulated environment, every document passes through a verification process that confirms accuracy and consistency. For patient-facing instruments \u2014 consent forms, patient diaries, patient-reported outcome (PRO) questionnaires \u2014 linguistic validation ensures the text is understood correctly by its intended audience, and where necessary comprehension testing with patients is added to the process. Indication-specific glossaries keep terminology consistent throughout the study, and every text is edited by an independent editor. Keeping that terminology up to date when the protocol changes is a detail that is often overlooked \u2014 and a critical one.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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01 \/ ANALYSIS<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Document Analysis<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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The type of document, its target audience, and its intended use within the clinical trial are evaluated.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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02 \/ TERMINOLOGY<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Terminology Management:<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Throughout the study, consistency across documents is maintained by using indication-specific terminology glossaries.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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03 \/ TRANSLATION<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Professional Translation<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Content is translated with due consideration for scientific accuracy and the target reader\u2019s needs.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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04 \/ EDITORIAL<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Independent Editorial Review<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Every text is reviewed by an expert editor who is independent of the translator.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Keeping terminology up to date when the protocol changes is a detail that is often overlooked but critical.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Common mistakes<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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What kinds of errors in clinical trial translation can cause problems?<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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The problems most often encountered in this field are: translating patient-facing text in a scientific register and losing comprehensibility; failing to update terminology after protocol amendments and creating inconsistencies between documents; translating CRF field names without aligning them with the database; not adapting dates, units and decimal separators to the target country; and ignoring the format and heading structure the ethics committee expects. Any one of these can delay the study or send a document back.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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\n\t\t\t\t\t\tFailing to update the terminology following protocol changes and creating inconsistencies across documents.\t\t\t\t\t<\/p>\n\t\t\t\t\n\t\t\t<\/div>\n\t\t\t\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\tTranslate CRF domain names without matching them to the database.\t\t\t\t\t<\/p>\n\t\t\t\t\n\t\t\t<\/div>\n\t\t\t\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\tFailing to adhere to the format and heading structure expected by the ethics committee.\t\t\t\t\t<\/p>\n\t\t\t\t\n\t\t\t<\/div>\n\t\t\t\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Experience and Process<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Over 30 years of expertise in medical translation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Specialising in medical translation for over thirty years, Mirora ISO 9001 certified, with an ISO 17100-aligned workflow is the translation partner of choice for leading pharmaceutical companies and clinical research organisations.<\/p>

Throughout the study, indication-specific terminology glossaries ensure consistency, and each text is reviewed by an independent editor.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Case Study<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Case study: three years of a partnership spanning more than a decade<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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We have worked with an international pharmaceutical organisation for more than ten years. In the past three years alone, and for this client alone, we completed 1,385 projects and translated more than 3.9 million words, handling the documents of 76 to 81 clinical studies each year.<\/p>

Throughout this period a single terminology glossary was used across all projects, and every document was reviewed by a specialist editor independent of the translator.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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10+ years<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Ongoing collaboration<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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1.385<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Projects over the past three years<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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3,9M+<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Translated word<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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76\u201381<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Annual clinical study<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Glossary of Short Terms<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Key Terms Used in Clinical Trial Translation<\/h2>\t\t\t\t<\/div>\n\t\t
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ICF<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Informed consent form.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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CRF \/ eCRF<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Case report form and its electronic version.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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CSR<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Clinical trial report.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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IB<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Researcher Brochure.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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IRB \/ Etik Kurul<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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The committee that approves patient-related documents.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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GCP<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Good Clinical Practice.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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PRO<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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The test result reported to the patient.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Sponsor<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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The organization that initiated and funded the study.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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CRO<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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A contract research organization conducting the study on behalf of the sponsor .<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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FAQ<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Frequently Asked Questions About Clinical Trial Translation<\/h2>\t\t\t\t<\/div>\n\t\t
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Why is clinical trial translation a specialism of its own? <\/div><\/span>\n\t\t\t\t\t\t\t\n\t\t\t<\/path><\/svg><\/span>\n\t\t\t<\/path><\/svg><\/span>\n\t\t<\/span>\n\n\t\t\t\t\t\t<\/summary>\n\t\t\t\t
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Strict regulatory oversight, many document types and the additional verification steps expected for patient-facing materials set it apart from general medical translation.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/details>\n\t\t\t\t\t\t

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Which documents are translated? <\/div><\/span>\n\t\t\t\t\t\t\t\n\t\t\t<\/path><\/svg><\/span>\n\t\t\t<\/path><\/svg><\/span>\n\t\t<\/span>\n\n\t\t\t\t\t\t<\/summary>\n\t\t\t\t
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Mainly the protocol, the investigator\u2019s brochure, the informed consent form (ICF), the case report form (CRF), patient diaries and the clinical study report (CSR).<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/details>\n\t\t\t\t\t\t

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Why is back-translation requested for consent forms? <\/div><\/span>\n\t\t\t\t\t\t\t\n\t\t\t<\/path><\/svg><\/span>\n\t\t\t<\/path><\/svg><\/span>\n\t\t<\/span>\n\n\t\t\t\t\t\t<\/summary>\n\t\t\t\t
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Because a consent form is addressed directly to the patient, it is essential to confirm the meaning has been conveyed correctly; an independent back-translation is therefore carried out on request, usually followed by ethics committee approval.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/details>\n\t\t\t\t\t\t

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How do protocol amendments affect terminology? <\/div><\/span>\n\t\t\t\t\t\t\t\n\t\t\t<\/path><\/svg><\/span>\n\t\t\t<\/path><\/svg><\/span>\n\t\t<\/span>\n\n\t\t\t\t\t\t<\/summary>\n\t\t\t\t
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A trial does not stand still; terminology has to be updated with every amendment, otherwise inconsistencies appear across documents.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/details>\n\t\t\t\t\t\t

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What is the most critical point in CRF translation? <\/div><\/span>\n\t\t\t\t\t\t\t\n\t\t\t<\/path><\/svg><\/span>\n\t\t\t<\/path><\/svg><\/span>\n\t\t<\/span>\n\n\t\t\t\t\t\t<\/summary>\n\t\t\t\t
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That field names match the database exactly; a single differing term causes confusion in data entry and analysis.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/details>\n\t\t\t\t\t\t

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Which standards matter most? <\/div><\/span>\n\t\t\t\t\t\t\t\n\t\t\t<\/path><\/svg><\/span>\n\t\t\t<\/path><\/svg><\/span>\n\t\t<\/span>\n\n\t\t\t\t\t\t<\/summary>\n\t\t\t\t
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ICH Good Clinical Practice, the EU CTR, ICH E3 (report structure) and ISO 9001\/17100; buyers prefer providers that work in line with these frameworks.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/details>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Discuss your clinical research translation project with Mirora<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Please share the scope of your clinical research documents, language pairs, and project requirements with us. From the protocol to the ICF and CRF forms, and from patient diaries to clinical trial reports, let\u2019s work together to plan a translation process tailored to your needs.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

\n\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tContact Us About Your Project \u2192<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"

Medikal ve Ya\u015fam Bilimleri Klinik Ara\u015ft\u0131rma \u00c7evirisi Klinik ara\u015ft\u0131rma \u00e7evirisi, bir klinik \u00e7al\u0131\u015fman\u0131n y\u00fcr\u00fct\u00fclmesi i\u00e7in \u00fcretilen t\u00fcm belgeleri kapsar: \u00e7al\u0131\u015fman\u0131n…<\/p>","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"footnotes":""},"class_list":["post-23657","page","type-page","status-publish","hentry"],"yoast_head":"\nKlinik Ara\u015ft\u0131rma \u00c7evirisi Nedir? | Mirora<\/title>\n<meta name=\"description\" content=\"Klinik ara\u015ft\u0131rma \u00e7evirisi: belge t\u00fcrleri (protokol, ICF, CRF, CSR), reg\u00fclasyon \u00e7er\u00e7eveleri (EU CTR, ICH-GCP), dilsel do\u011frulama ve s\u0131k yap\u0131lan hatalar.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/mirora.com\/en\/clinical-trial-translation\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Klinik Ara\u015ft\u0131rma \u00c7evirisi Nedir? 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