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Freelance translator and/or interpreter, Verified site user
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Bio
I started my translation business in 2001, decided to specialise in medical translation in 2004 and since 2009 I have been providing medical translation, validation and regulatory submission file (CTD/variation submissions) preparation services to the local and global translation companies, contract research organizations and pharmaceutical companies. I have completed training courses on regulatory affairs, GMP, GCP, CTD preparation, application types and requirements, thinking that by better understanding the regulations governing the life sciences industry, I will provide better quality translation services and facilitate communication between companies and authorities/patients. I also closely follow the announcements of the Ministry and competent authorities regarding the types of documents I translate. I am an experienced translator who knows that meeting deadlines is as critical as translation quality, believes in the importance of uninterrupted communication with the client and enjoys her job. For more information, please see my CV and feel free to contact me.
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Expertise