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Writing
Medical Information

 

I create Frequently Asked Questions (FAQ), Product Q&As, and Standard Response documents (SRDs).

I write Informed Consent forms for patients participating in clinical trials and guidelines.

Writing Medical Information for the pharmaceutical industry

 

When therapeutics are approved and enter the market, Medical Information Departments are in demand to answer the questions of doctors, patients, and healthcare professionals. I support this process in writing FAQ documents - I research scholarly articles, clinical study reports, and other regulatory documents to write accurate and comprehensible content in audience-specific language. Through my former employment with a CRO, I have a thorough understanding of clinical trial regulation and pharmaceutical product life cycle management, so I am used to working with the documents and databases that these involve.

I also write informed consent forms and guidelines for patients who should be informed in detail about the therapy's benefits, applications, and risks.

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