As clinical trials and regulatory procedures become more complex it is becoming increasingly more important for healthcare companies to produce well-structured documents that present information clearly and concisely. This demand for the clear articulation of medical science drives a demand for well written, standard-compliant documents that medical professionals can easily and quickly read. At R&G our Medical Writing team works closely with our Regulatory and Statistical teams to provide our clients with professional, high-quality deliverables that are compatible with ICH guidelines and other applicable regulatory requirements.
Our Medical Writing Services Include:
The R&G Translation Center specializes in medical translation and is committed to providing our clients with professional, high-quality translation services.
The Translation Center has access to more than 100 medical translators, >90% of whom have a Master’s degree or higher. Our services cover all medical fields including R&D, registration and post-market surveillance dossiers for pharmaceutical, medical device and biological products. We can also assist clients with the translation of training, legal and regulatory & policy documents, too. We provide multi-lingual services for translations between English, Chinese, Japanese and French, etc.
Relying on the large talent pool at R&G, our Translation Center can also provide clients with professional proofreading services. All proofreading is conducted by experts in the relevant fields.
To guarantee the quality and consistency of our translations, we strictly adhere to our quality assurance system and have built a custom-tailored data bank. Furthermore, all translations are reviewed by our translation director of more than 7 years’ experience before being sent to clients.
If you would like to learn more about R&G, please download our brochure or feel free to contact us directly.