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I am a Medical Doctor with eight years of experience in the medical device industry. My personal track record in REGULATORY WRITING includes over 15 clinical evaluation reports (CERs) for class IIb and class III devices. I have a great deal of experience in both product development (clinical support for risk management or functional and design requirements) and post-market surveillance (post-market updates for clinical evaluations). I hold the respective certificates by the Notified Body TÜV and work in accordance with the Medical Device Directive, the relevant standards, and the most recent guidelines.
My experience in MEDICAL COMMUNICATIONS includes the creation of publication manuscripts, white papers, conference posters, abstracts, scientific brochures, speakers slide decks, sales presentations, surgical techniques, training material, medical website content, and more. My in-depth knowledge on PubMed and other search engines allows me to support you with any kind of scientific literature search and add evidence-based value to your medical communications.