EMTEX, founded in 2001, is an independent and compact company that offers professional medical writing services all around the world to the biotechnology, pharmaceutical, food and medical device industry.
Visit our website for more information: https://www.emtex.be
Emtex medical writers have the required know-how and skills to provide you with professional medical writing services across a wide variety of therapeutic fields.
Regulatory medical writing means creating the documentation that regulatory agencies require in the approval process for drugs, devices and biologics. Regulatory documents can be huge and are formulaic. They include clinical study protocols, clinical study reports, patient informed consent forms, investigator brochures and summary documents that summarize and discuss the data a company gathers in the course of developing a medical product. Below you can find an overview of the most common document types EMTEX writes:
Medical communications means writing documents about drugs, devices and biologics for general audiences, and for specific audiences such as health care professionals. These include sales literature for newly launched drugs, data presentations for medical conferences, medical journal articles for nurses, physicians and pharmacists, consumer education and programs and enduring materials for continuing education or continuing medical education. A few of the document types in this area are:
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