Piedmont Medical Writers LLC

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Our Services

We specialize in creating documents for regulatory purposes and for
medical communications. We can provide deliverables that have undergone QC review by a independent reviewer as well as stand-alone QC review of your documents.

Regulatory

  • Clinical study reports (Phases I - IV)
  • Investigator brochures
  • Safety and efficacy summaries
  • Clinical sections of CTDs
  • Clinical protocols and informed consents
  • Clinical trial registry summaries
  • INDs and IND annual reports

Medical communications

  • Posters (large format)
  • Abstracts
  • Slide sets
  • Clinical and preclinical research manuscripts
  • Annotated bibliographies
  • Review papers
  • CME course materials

Copyright 2010 Piedmont Medical Writers LLC