Pharmaceutical Medical Writing

QA Data offers a comprehensive pharmaceutical medical writing service for a wide range of documents including protocols, clinical reports and publications. Our highly experienced team of medical writers will professionally prepare reports in accordance with current regulations and guidelines suitable for submission to regulatory authorities.

We understand the importance of well written documents. From protocol to Clinical study reports or abstracts and publications, our goal is to produce concise, meaningful, and polished clinical documents, at the same time offering our clients a cost-effective solution.

Our skilled writers have the relevant scientific/medical education, and experience to produce expertly-written documents – on time. We strive for precision, clear presentation and scientific accuracy. Prior to delivery, all our documents undergo a rigorous QC review to ensure they look good, read well, accurately interpret the study results, and comply with regulatory and sponsor approved /provided stylistic guidelines.

Our medical writing expertise include the following:
• Protocols
• Clinical study reports
• Clinical sections and summary sections of Common Technical Documents (CTDs)
• Clinical sections and summary sections of New Drug Applications (NDAs)
• Abstracts, presentations, and journal articles
• Investigator brochures
• Informed consent forms
• Expert reports and executive summaries
• Written and tabular summaries
• Medical and scientific literature reviews
• Safety narratives, Investigational New Drug Applications (INDs)

Our medical writing is offered as a follow-on to our data management or as a stand-alone service.

For more information or to discuss pharmaceutical medical writing please contact us directly.