Professional
Medical Device Translation
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Need for expert medical device translation
With strict MDR language requirements, medical device translation has become a compulsion to produce and import medical devices in countries of the European Union.
Accurate translation is essential for all stakeholders involved in the process, from manufacturers to regulatory authorities and medical professionals. It helps overcome language barriers at various stages and facilitates effective communication.
According to a study on language barriers in healthcare, 50% believed that language barriers contributed to a higher risk of errors. This emphasizes the necessity for accurate translation services in the medical industry.
We provide medical device translation for any device
Diagnostic devices
Imaging Devices
Surgical instruments
Monitoring Devices
Rehabilitation devices
Dental devices
Prosthetics
Implants
Endoscopy devices
Orthopedic devices
Respiratory devices
Cardiovascular devices
We consider the ISO 17100 certification important and demonstrate our commitment to the needs of our customers worldwide.
EU MDR TRANSLATION REQUIREMENTS
It is the responsibility of the manufacturers to comply with translation requirements and provide translations of all necessary documents accompanying the device in one or more official languages of the EU member states. The translated materials must be precise, and the source language must also be clear.
The primary information commonly required includes product details like labelling, packaging, and Instructions for Use (IFU). Other information, such as user manuals, product safety documentation, etc., are also subject to language requirements.
With our team of expert professionals and the use of advanced technologies, we can provide precise translations that comply with MDR.
Accurate Medical device Translation for any document
- Medical device packaging
- Medical device labelling
- Instruction for Use (IFUs)
- Medical device operation manuals
- The user interface for medical software
- Safety data sheets (SDS)
- Regulatory documents
- Marketing materials
- Clinical training materials
- Patents
- Intellectual Property Documents
Choose from 70+ languages
98% OF OUR CLIENTS SAY THEY WOULD RECOMMEND OUR SERVICES TO A COLLEAGUE
Powered By Technology Translated By Humans
Machine Translation
Language Intelligence
Terminology Management
Automated Tracking
A RELIABLE PARTNER FOR ALL YOUR LANGUAGE TRANSLATION NEEDS
We have a robust process in place, including proofreading, editing, quality assessment, and typesetting to ensure our translations are of the highest quality.
If you are looking for a dependable translation partner for your manufacturing translation, we are here to help.
By partnering with us, you get –
- A dedicated project manager for each project
- Native translator with domain expertise
- Quality assessed accurate translations delivered on time
- Unlimited revisions to translated content based on your feedback
- Translation certificate accepted by all regulatory authorities
Order your Medical device translations here
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FAQS ON MEDICAL DEVICE TRANSLATION
How much do medical device translation services cost?
How long does medical device translation take?
Can you handle the translation of medical device documentation according to MDR guidelines?
Our team is well aware of MDR’s intricacies and is well-versed in the terminology, documentation requirements, and translation standards demanded by MDR. We are also ISO 17100 certified and we provide a digitally signed certificate that can be used for regulatory purposes.
How do you ensure that the translations meet MDR requirements?
We ensure that our translations align with MDR standards, helping our clients navigate regulatory challenges seamlessly.