We apply the technical knowledge and know-how cultivated over many years in the manufacturing sectors of "medical devices" and "precision instruments" to the field of translation as well.
We promise reliable accuracy and high quality, backed by the technical know-how we have cultivated over many years in the manufacturing industry! Our multilingual staff is not only proficient in languages but also well-versed in the specialized terminology used in medical devices and precision equipment manufacturing, as well as the workflow, to support our customers. Leveraging our experience in dealing with multinational companies, we provide high-precision [manufacturing industry] technical translations that meet our customers' needs from a global perspective. We have extensive experience and a proven track record in technical translation, covering everything from the terminology of equipment screen interfaces to product manuals, specifications, and design documents.
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basic information
Main Handling Documents - Translation of manuals (user guides) - Translation of specifications - Translation of online help - Translation of websites - Firmware / Software localization Supported Languages English, Chinese
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Applications/Examples of results
Technical translations of various documents such as product manuals, specifications, and design documents from the terminology of the machine's screen interface.
Company information
Our company manufactures mass-produced devices related to specimen testing automation systems, in addition to probes that connect to ultrasound diagnostic devices essential for advanced medical imaging examinations. We specialize in precision mounting technology (fine soldering) using microscopes, maintaining a unique position in the increasingly automated world of mounting. Additionally, we offer technical translation services for various specifications and manuals. *Design and development are handled by our parent company, Mirapro Co., Ltd. We obtained ISO 9001 certification, the international standard for quality management systems, in June 2013, and we implement thorough quality control throughout all processes to produce products of the highest quality. Furthermore, as a contract manufacturer of medical devices, we acquired ISO 13485, the international standard for quality management systems related to medical devices, in August 2014, and on October 30, 2017, we were registered as a medical device manufacturer in accordance with Article 23-2-3, Paragraph 1 of the Act on Securing Quality, Efficacy, and Safety of Pharmaceuticals and Medical Devices.
