35 years experience in the Medical Device industry. I have been involved with developing submissions to the FDA, European Notified Bodies and to other countries in the global marketplace. My experience includes working with marketing departments to develop materials for internal and external use. I have extensive experience working with technical personnel for whom English is a second language. I can write and review such work as to bring it to technically correct without spending undo time on grammar etc or the documents can be cleaned for technical content and proper sentence structure along with other desired content.