MEDICAL WRITING SERVICES

Knowing how to communicate in the scientific and medical field is a crucial aspect and a competitive benefit for companies in the sector. ASTW medical writing services are provided by highly qualified medical writers with experience in all clinical and therapeutic fields, and guarantee privacy and confidentiality.
All of the professionals of the ASTW medical area team have a degree in medicine, or a master’s degree or doctorate in pharmacy, biology and at least 10 years of experience in editing medical documents.

What are you looking for?

The right formula for your texts.

WE WORK IN ALL CLINICAL AND THERAPEUTIC SECTORS

A vast network of professional medical writers, each specialised in a specific clinical and therapeutic area:

MEDICAL WRITING SOLUTIONS

  • Writing of original articles (scientific/clinical) for publication in peer-reviewed journals
  • Systematic literature review
  • Revision of scientific manuscripts in English
  • Creation of abstracts, presentations and posters for conferences
  • Production of informative materials and educational slides
  • Opinion leader sourcing
  • Organization of online and residential courses
  • Content creation for company websites
  • Drafting of scientific articles and informative texts
  • Creation and sending of newsletters
  • Scientific publication planning and editorial planning
  • Manuscript formatting in line with specific journal guidelines. Creation of cover letters and assistance with referee comment response
  • Drawing up of tables and figures
  • Writing and revising book chapters
  • Linguistic review and translation of scientific texts

REGULATORY WRITING SERVICES
Our Regulatory Medical Writing services include:

  • Clinical study reports (complete, abbreviated or synoptic, CSR in compliance with ICH E3)
  • Clinical study report appendices
  • Clinical study protocols and protocol revision
  • Investigator dossiers (IB)
  • Patient histories
  • Safety update reports
  • IND documentation
  • Summary documents for new drug authorization applications and marketing authorization applications (NDA / MAA) – eCTD modules 2.5 and 2.7
  • Data Safety Management Board (DSMB) reports
  • Clinical development plans
  • Principle objective outcome reports
  • Informed consent
Request a quote

Contact us to tell us about your project, and we will find the solution that best suits your needs. We provide free quotes.