Clinical trials
In Hungary, hundreds of clinical studies are conducted each year, with the number of planned studies exceeding 300 annually (source: Hungarian Institute of Pharmacy, 1993–2013).
The authorization and processing of clinical trials often take a considerable amount of time, during which numerous translation tasks may be required. These include translating documents for authorization as well as the documentation generated after the conclusion of the trials.Additionally, many translation requests can arise throughout the course of the examinations themselves.
In Hungary, hundreds of clinical trials are underway each year, with over 300 new trials planned annually (source: Hungarian Institute of Pharmacy, 1993–2013). The authorization and processing of these studies often take a considerable amount of time, during which numerous translation tasks may arise. These include translating documents required for authorization as well as the documentation generated after the conclusion of the trials. Moreover, many additional translation requests can emerge throughout the course of the examinations.
It is essential that translated documents accurately reflect the demographic characteristics of the patients participating in clinical trials, remain clear and understandable, and comply fully with the stringent regulations set by the relevant authorities. LinguaMED Translation Agency supports you in achieving this by providing precise and professional translations of all documentation required for clinical studies. We offer comprehensive medical language services to companies and institutions conducting research at every phase, whether involving medicines or medical devices. Our expert team includes doctors, healthcare professionals, pharmacists, and lawyers qualified as medical translators. This collaboration ensures outstanding quality combined with the best balance of price and value.
We offer translation (not only) of the following documents:
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- Promotion for patient recruitment in clinical trials
- Documentation needed for authorities
- Personal data sheet(s)
- Clinical trial report(s)
- Agreements with the patients
- Study user guides
- Monitoring reports
- Information consent form
- Periodic reports
- Clinical trial plans
- Questionnaires
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Request for a quotation regarding clinical trial documentation here.