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