Nancy Milligan Medical Ltd
Nancy Milligan Medical Ltd


At Nancy Milligan Medical I offer a full range of high-quality medical writing services in order to meet all of your clinical regulatory and medical communications needs.

Regulatory documents:

  • Clinical study protocols (CSPs) and protocol amendments
  • Common technical document (CTD):
    • Clinical study reports (CSRs), including abbreviated reports (Module 5)
    • Clinical summaries (Module 2)
    • Clinical overviews (Module 2)
  • Investigator's brochures (IBs)
  • Patient safety narratives

Medical communications documents:

  • Manuscripts for publication in peer-reviewed medical journals, including:
    • Primary research papers
    • Narrative and systematic reviews
    • Submission and liaison with journal editors
  • Literature searches and reviews
  • Publication summaries
  • Slide presentations
  • Abstracts and posters
  • Conference reports and summaries
  • Competitor reviews
  • Product brochures and monographs
  • Website materials

  • Medical education materials

  • Product marketing materials

  • Training manuals

Nancy Milligan Medical also offers the following services:

  • Editing and proofreading

  • Quality control (QC) checking

  • Editing or rewriting non-native English

  • Reference audit and mark-up

  • Key opinion leader (KOL) mapping

  • Conference attendance

  • Supervision or advising junior and non-native English speaking medical writers

  • Project management

I am also used to and comfortable tackling new projects, i.e. I can adapt quickly to types of documents I haven't worked on before or unfamiliar therapeutic areas, with the help of document guidelines or background research to get up to date on new topics. I am used to researching and reviewing complex scientific information.

I can provide a fixed cost for a project or work to an hourly or daily rate, which can be flexible depending on the type of work and your budget.

I also work with a network of companies and other freelancers for collaboration on larger projects or independent QC check of regulatory documents.

Through attending regular training and following regulatory guidelines or instructions for authors, I aim to uphold current ethical standards in medical writing.

Contact us

If you have any queries or require a cost estimate, please contact us:

+44 (0)7747 612651

Or use the contact form

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