Medical writing

From standalone to full-service projects, our experts provide a flexible medical writing service to deliver well-structured content that communicates the right message. We apply our wealth of experience from the pharmaceutical industry and academia across multiple therapeutic areas and product types to develop your regulatory documents and scientific publications to deadline, saving you time and money.

Our dedicated writing team works with you at every stage, from the initial trial conceptualization (protocol outline) through to approval (developing the full suite of CTD-compliant clinical submission documents).

The right documentation. Right on time.

Whether regulatory documents or scientific publications, our medical writers excel in understanding each document’s unique scope and requirements. Thus, we deliver standards-compliant clinical documents that can help you open doors to the future success of your project.
Our regulatory writing experts are here to develop your:

Protocols
Study Reports (CSRs and NSRs)
Investigator’s Brochures (IBs)
Clinical submission documents
Briefing documents
Layperson summaries
Pediatric Plans (PIPs and PSPs)
O&A documents
Device Documents: CIPs, CIRs, and CERs

Our publication experts can help you create awareness of your results, innovations, and discoveries in the scientific community.

Manuscripts for peer-reviewed journals
Systematic literature reviews and meta-analyses
Conference abstracts, posters, and oral presentations

Our knowledge spans all study phases, multiple therapeutic areas and product types including small molecules, recombinant proteins, gene therapies, oncolytic viruses, photodynamic therapy and modified stem cell transplantation.

WHY WORK WITH US?