Medical Writing

Expert Medical Writing for Your Every Need

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?

Meeting deadlines. Adhering to standards. Communicating the right messages, clearly and concisely. We are here to help you succeed.

10+ Years

Medical Writing Experience

17+ Years

Pre-clinical and Clinical Research Experience

PhD Level Experts

Deeply Rooted in Science

Broad Therapeutic Experience

Oncology and Rare Disease

Protocol Writing

Extensive Experience for Early and Late Phase Trials

<10 Weeks

CSR Turnaround Time

Supporting Resources

Resources

Get in touch

Let’s support you on your next project