Medical writing

Medical writing is established in pharmaceutical industry, because it requires special skill to produce well-structured documents hat present information clearly and concisely. Medical writing for pharmaceutical industry can be classified as either regulatory medical writing or educational medical writing. Regulatory medical writing means creating the documentation that regulatory, which include clinical protocols, clinical study reports, patients informed consent forms, investigator broachers and summary documents.

Educational medical writings mean writing documents about drugs, devices and biologics for healthcare professionals. These contain sales literature for newly launched drugs and data presentations at conferences.

 

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