Our medical writingsolutions are designed to support your clinical trial, regulatory, and publication writing needs.
We deliver high quality documents in a timely manner, while offering our clients the flexibility to choose between our full-package writing service and single-document writing and revision.

From Clinical development to post-marketing studies...
We supportour clients starting with study design in collaboration with key experts in different therapeutic areas, through the whole study, offering Clinical Study Protocol, Informed Consent Forms, Clinical Study Report, and Patient Narratives writing services.
Our servicesinclude the preparation and update of Regulatory Documents such as Investigator Brochure (IB), Common Technical Dossier (CTD) & eCTD, and Investigational Medicinal Product Dossier (IMPD).
We supportour clients in different publication types, handling the whole process of writing publications and scientific journal submissions, while handling revisions and responding to reviewers/editors.
Our servicesalso include Advisory Board Meeting minutes reporting and Medical Translation Services for different material

Our Medical Writing Services includes

Study Design


CRF Design & eCRF

Informed Consent Writing & Translation

Clinical Study Report

CTD writing and eCTD formatting and submission

Investigator Brochure



Submission to Medical Journals of High Impact Factor and Follow up till acceptance

Patient Leaflet

Poster Design

Advisory Board attending and Reporting

Medical Translation