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Fueled by new technologies and innovations, the medical device industry has become one of the largest and fastest-growing industries in healthcare. That’s why accurate medical device translation services begin to come into play.
Medical device translation refers to the professional translation and localization of technical and marketing documents, instructions for use, packaging and labeling materials, and even software in the process of launching a new product or device in a foreign market. It’s an integral part of the medical device launching, regulatory compliance, and approval process.
Medical device translation should be accurate, precise, and certified.
As a certified medical translation company with the headquarter in the US, 24 Hours Translate provides technically precise and culturally accurate medical device translation and localization services in 85 other languages, including in English, Spanish, German, Chinese, French, Japanese and other major European, Asian, Scandinavian and Middle-Eastern languages.
We have the linguistic and medical-expert team to undertake multiple language translation projects, such as translating one English medical device directive into 8, 20 or even 35 languages.
Are you working for a medical device company or manufacturer in need of certified and high-quality translation services for your critical medical device documents? Then 24 Hours Translate is the best medical and healthcare translation partner for you.
We are a professional medical translation company that provides accurate, 100% human-powered, HIPAA-compliant medical device translation services in over 85 languages. We help the leading medical device companies and manufacturers worldwide overcome language barriers, regulatory compliance challenges in different foreign countries, and gain more success in the international market.
Medical experts have an excellent command of medical terminology and subject matter expressions in the medical and healthcare sectors. They also understand the increasingly strict regulatory requirements issured by the European Union (EU), US FDA, and other governmental regulatory bodies on the translation and presence of medical device labelling, packaging, instructions for use, marketing materials and other information.
Getting healthcare and medical experts involved in the translation review process is an effective way to help medical device companies reduce non-compliance risks and quickly respond to market opportunities. That’s why 24 Hours Translate deploys that every piece of your medical device documents is translated by our qualified human medical translators and reviewed by our signed medical experts to deliver the highest level of accuracy, precision, and validation.
We promise that your medical device documents will be securely handled, carefully translated and validated by medical experts.
The European Union (EU), US FDA, and other regulatory bodies have set strict regulatory requirements and approval processes for the entry of new medical devices into local markets. Medical device manufacturers and distributors must efficiently adapt to the document compliance provisions and their language requirements to avoid compliance issues and successfully launch their products and devices to the targeted markets on time.
In 24 Hours Translate, our team is happy to offer country-specific, cost-effective translation and localization solutions for your specific translation needs and challenges regarding meeting the language requirements in different markets. Our medical device translation services cover various types of medical device information, including medical device labeling, packaging, instructions for use, marketing materials, software, and user interfaces:
Instructions for Use (IFU) refers to the document which contains key information about the medical device, such as the intended purpose, operating specifications, target patients, safety and clinical performances, and precautions.
IFU and its translation must meet strict regulatory requirements to obtain market entry. According to the European Union, all documentation including an IFU must be properly translated into the 24 official languages of the European Union to get the CE Mark, which will guarantee that medical device manufacturers and distributors can sell the medical device throughout the European Economic Area (EEA).
As a certified translation vendor for medical device companies, 24 Hours translate has a professional team of qualified medical translators, medical-expert editors and reviewers with regulatory compliance knowledge and technical expertise for different regions to deliver accurate and valid IFUs translation services in 85 languages. We ensure our translations are:
Accompanied by the medical device that is put up for sale, medical device labels also play an important role in giving patients, medical professionals, and other end-users direct, clear instructions and warnings to guide proper use and ensure safety.
The international medical device industry must implement the best practices in the design and writing of labels and properly translate the labels into the required official languages to meet regulatory requirements. This is also a crucial part of the successful launching of medical devices.
24 Hours translate provides clear, accurate, and regulatory-compliant medical device label translation services for international medical device manufacturers and traders. Contact us to get your country-specific, medical device translation solutions!
Driven by technological innovations, the medical device industry is going through a digital transformation in recent years. Medical device manufacturers and their software developers are making their traditionally static devices more digital, smart, and convenient for patients, doctors, physicians and end-users to use.
When medical device companies are expanding their business overseas, they will need to not just translate their medical device documentation, but also localize their medical software. The software needs to be localized and adapted to the languages, cultures, the user interface (GUI), times, terminology and measurement systems of the target markets.
That’s why medical device manufacturers need a professional human translation team to assist their software localization process. As a certified, 100% human-based medical translation company, 24 Hours Translate provides accurate, high-quality software localization services.
We have a professional team of certified medical translators, medical-expert editors, and reviewers with regulatory knowledge and technical expertise to assist international medical device manufacturers and traders overcome language, cultural, technical, and market-entry barriers and gain more success in the global market.
Under the new EU MDR, proper translations of medical device content are playing a bigger role in the manufacturer’s efforts to pass its conformity assessment and obtain a CE marking in the European Union. Medical manufacturers need to work more proactively with their translation vendors to increase the accuracy of their device labeling, Instructions for Use (IFU) and other safety information.
The following 5 points should be highlighted when it comes to the translation requirements of medical devices under the EU MDR:
As a professional translation vendor in the medical device industry, 24 Hours translate provides accurate, precise, and country-specific medical device translation and localization services in over 85 languages, including English, Spanish, Chinese, German, French, Japanese, Korean, Arabic, Indonesian, African languages and other major European and Asian languages.
24 Hours Translate offers 100% human-powered, regulatory-compliant, best-in-class Spanish medical device translation services, including Spanish to English, English to Spanish, Spanish to Chinese, Spanish to German, and other Spanish-based language pairs.
We have a large team of experienced, professional, native in-country Spanish medical translators and reviewers who have a deep understanding of local culture and an excellent command of medical terms, jargon, and other complicated phrases used in Spanish medical device labelings, IFUs, directives, and other documentation.
We are committed to providing the best Spanish medical translation services to international medical device manufacturers, traders, and distributors around the globe.
24 Hours Translate offers the most competitive and affordable translation prices for our customers in medical and healthcare industries, with prices starting at $0.09 per word for professional medical document translation and review.
Talk to us to get the specific rates per word for professional medical records translation services, depending on your language pairs, time and other requirements.
We are happy to provide price discounts for your large-scale medical documents and content translation projects. Learn more about our full pricing information.
24 Hours Translate is a professional translation and localization service provider with customers and projects around the globe. We have been providing 100% human-powered certified translation services in over 85 languages and 30 industries of expertise.
Yes, We can. 24 Hours Translate can translate and output all types of medical device document formats upon request, including PDF, MS Word, PowerPoint, Adobe InDesign, Madcap Flare, XML, DITA, XLIFF, and many other electronic and digital formats.
Talk to us to get your medical device content carefully translated by our certified medical translators who are specialized in the medical fields and also have expertise in medical regulatory compliant knowledge.
Medical terminology is frequently used by healthcare professionals in almost all aspects of medical, healthcare clinical facilities. It refers to the words and phrases that are highly specialized and recognized within the medical field but can precisely describe diseases, illnesses, medical conditions, and diagnoses.
Medical terminology is an important part of the healthcare industry. Serving as a coding language of medicine, medical terms can efficiently help doctors, nurses, pharmacists, medical assistants, and even billing specialists understand what’s happening or what should be done to assist the patients.
EU MDR refers to the new European Union Medical Device Regulation. It’s a new set of regulations that govern the production and distribution of medical devices in Europe.
It officially came into force at the end of May 2021. It’s necessary for all medical manufacturers, distributors and companies to comply with the MDR regulations so that they can operate in the EU market.
The quick answer is yes. Starting on 26 May 2021, MDD was replaced by MDR.
The EU MDR is much longer and stricter than the previous MDD in terms of product safety, quality management, and the transparency of technical documentation.
There is a clear difference between medical translators and medical interpreters, although both work to provide effective multilingual communication and improve patient care and satisfaction in hospitals and many people still use these two terms mistakenly.
Medical translators work with written documents, such as translating medical device documents, medical directives, informed consent forms, notices of right or intake forms and any other letters or notices in written form. On the other hand, medical interpreters provide spoken or oral language services in healthcare facilities to ensure meaningful communication between patients and healthcare providers, such as doctors, physicians and nurses.
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