Medical Writing

Medical writing is one of the important areas in clinical research. Our medically qualified professionals bring their experience into the protocol design and writing such as Investigator Drug Brochure compilation, Clinical Report and Integrated Reports.
 ESMAR provides qualitative and accurate medical writing for clinical trials phase I-IV and bioequivalence studies as part of a full-service program or as a stand-alone service.
The ESMAR medical writing team provides support in the following areas:
- Medical writing of pre- and post-clinical research :
  ♦  Clinical study protocols
  ♦  Investigator’s brochures
  ♦  Patient informed consent forms
  ♦  CRF design
  ♦  Statistical reports and Clinical Study Reports
- Scientific articles, abstracts and clinical reports
- Study documentation for regulatory submission
- Drug marketing literature (Abstracts or slides for posters or presentations)
 
We assist our clients in their medical documentation for products development, using our scientific background and professional knowledge, flexibility, as well as team spirit!