Medical and Biotechnological Content, and Literature Reviews

 

When therapeutics and biotechnological products enter the market, Information Departments are in demand to answer the questions of doctors, patients, and customers. I support this process in writing FAQ and Standard Response documents - I research scholarly articles, clinical study reports, and other regulatory documents to write accurate and comprehensible content in audience-specific language.

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I also write informed consent forms and guidelines for patients who should be informed in detail about the therapy's benefits, applications, and risks, and plain language summaries (PLS) of clinical study reports.

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I have a thorough understanding of clinical trial regulation and the life cycle management of Medicinal Products and Medical Devices. I perform systematic literature reviews for your official reports. Since I have a deep and thorough professional background in cellular and molecular processes, genetics and genomics, I am especially skilled in literature search and reporting on molecular and cellular therapies and diagnostics. An education in intergrative health and nutrition allows me further to perform and understand literature recherche on the effect of nutritional molecules and hormones on the cellular and neuronal activity in the human body.

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