According to the U.S. Bureau of Statistics, the translation industry has been growing approximately by 42% since 2010 and this trend is believed to carry beyond 2020. Translation or specialized medical translation is one of the most significant services in the healthcare domain. From the pharmaceutical products and services to the intensive care unit documentation, medical translation services find a role in every sphere of the healthcare field.
Pharmaceutical companies, clinical research organizations (CROs), manufacturers of medical and surgical devices, biotech companies and medical managers require the services of medical translators. A specified Precision, medical background along with updated knowledge is called for while translating as they postulate a high degree of quality and even a slight lack in it may be a matter of huge concern. It also requires multiple levels of quality control and a full understanding of stringent laws, especially for the US, the European Union, and Japan.
Pharmaceutical companies, clinical research organizations (CROs), manufacturers of medical and surgical devices, biotech companies and medical managers require the services of medical translators. A specified Precision, medical background along with updated knowledge is called for while translating as they postulate a high degree of quality and even a slight lack in it may be a matter of huge concern. It also requires multiple levels of quality control and a full understanding of stringent laws, especially for the US, the European Union, and Japan.
Tradecom’s dedicated, diligent and adept team assures superb services by facilitating technically correct translation. With around 15 years of experience, Tradecom has made a mark in the medical transcription and translation industry. At Tradecom, we translate varied types of documents like toxicology reports, data sheets, IFU (Instructions for use), dossiers, IVR, investigator brochures, drug registration documentation.
Marketing collateral, clinical protocols, CRF (Case report forms), clinical trials, manufacturing process descriptions, Informed consent forms, Masterbatch reports and deviation reports, multimedia audio and visuals, scientific journal articles, regulatory audits, regulatory documents, pharmacological studies, patient-reported outcomes, patient information, package inserts and labels, corporate websites, patient recruitment materials, Quality of life(QoL) measures, SAE and SOP procedures, protocols, CRA training materials and videos, PRO (Patient-reported outcomes), questionnaires and adverse events.
Marketing collateral, clinical protocols, CRF (Case report forms), clinical trials, manufacturing process descriptions, Informed consent forms, Masterbatch reports and deviation reports, multimedia audio and visuals, scientific journal articles, regulatory audits, regulatory documents, pharmacological studies, patient-reported outcomes, patient information, package inserts and labels, corporate websites, patient recruitment materials, Quality of life(QoL) measures, SAE and SOP procedures, protocols, CRA training materials and videos, PRO (Patient-reported outcomes), questionnaires and adverse events.
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