Marketing your medical devices outside the country they were developed in, requires careful translation of all instructions and specifications. It can also require rebranding to account for cultural differences.
RIC International is a leading provider of medical, engineering, and technical translation services in the United States. We have an experienced team of medical translators and editors with impeccable linguistic skills, technical writing expertise, and – most important – professional degrees such as M.D. and Ph.D. in all major areas of life sciences, biomedical engineering, and medicine.
In addition to our team of dual-skilled translation professionals, our Quality Control Systems and Methodology are designed to meet the exacting demands of the medical, pharmaceutical, and medical devices industries. We provide for multiple rounds of proof-reading and editing by native speakers of the target language. Our highly skilled project managers ensure that deadlines are met without fail. Your project manager is available 24 hours a day, 7 days a week, to answer questions or address any concerns you may have.
For over 15 years, RIC International has been translating documents for the Medical and Surgical Devices Industry. We translate documents such as:
Over 500 Companies rely on RIC International to deliver precise, accurate translation of the most technical documents, on time and on budget. They range from Fortune 100 multinationals, such as Merck, Novartis, Tyco Healthcare, and Pfizer, to small and mid-size rapidly globalizing technology and biopharmaceutical companies, such as Amgen, Mettler-Toledo, and Tektronix.
We translate documents in 80 global languages, including all the major languages of Europe, Asia, South America, and the Middle East.
As a leader in quality translation services, RIC International provides a Certificate of Accuracy to all clients at no additional charge. The Certificate is issued upon request and can be prepared in electronic format or a notarized hard copy.
We also help medical and in-vitro diagnostic device manufacturers comply with the European Union's regulations for obtaining the CE Mark designation for their devices. Our product labels and instructions for use meet all requirements of EU directives for medical devices. See "Guidelines Relating to Medical Devices Directives of the European Union", especially Directive 2.5/5 on Medical Device Labelling Translation Procedure.
RIC International is a US-based global translation company. We focus exclusively on providing highest quality medical, engineering, and technical translation services to our corporate clients. Our specialization, focus, industry-leading quality management standards, and customer-centered attitude have earned us the trust of many of the world's best technology and biomedical companies.
Please call us at 800.240.0246 or e-mail to info@ricintl.com to find how RIC International can help you meet your translation requirements.