Medical writing services for pharmaceutical companies
Our medical writing services can create accruate and high quality documents across therapeutic areas, phases of development, and product types.
With growing demands for transparency in clinical trials and pharmaceuticals, medical writing is crucial.
Pharmaceutical Medical Writing
From standalone to full-service projects, our experts provide a flexible medical writing service. We deliver well-structured content that communicates the right message. By applying our wealth of pharmaceutical experience, we can write across multiple therapeutic areas and product types. We’ll help you to develop your regulatory documents and scientific publications, saving you time and money.
Our team delivers quality documents quickly, accelerating your submissions. We work 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.
Check out our experts interview!
Why work with us? Specialised medical writing for pharma & biotech
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
How can we support your next project?
Whether you’re looking for a protocol review or a proposal,
simply reach out to us by filling our request for proposal.
