Medical writing services for pharmaceutical and biotech companies
Our medical writing services can create accurate and high-quality documents across therapeutic areas, phases of clinical development, and product types.
With growing demands for transparency in clinical trials and pharmaceuticals, medical writing is crucial.
Pharmaceutical Medical Writing
Aixial Group offers flexible medical writing support, from standalone documents to fully integrated, full-service programs. Our experienced medical writers produce high-quality, scientifically sound content tailored to your audience—whether for regulatory authorities, ethics committees, or the scientific community.
With deep pharmaceutical expertise and cross-functional collaboration, we deliver accurate, well-structured documents across a broad range of therapeutic areas and product types. From early-phase protocols to full CTD submission packages, we support you at every stage of development—streamlining timelines, ensuring compliance, and accelerating your path to approval.
The right documentation. Right on time.
Whether regulatory documents or scientific publications, our medical writers excel in developing each document’s unique scope and requirements. With a strong foundation in global standards and therapeutic knowledge, we deliver high-quality, compliant clinical documents that support the success and advancement of your clinical program. Our regulatory writing experts are able to support the development of:
- Protocols
- Study Reports (CSRs and NSRs)
- Investigator’s Brochures (IBs)
- Clinical submission documents
- Briefing documents
- Layperson summaries
- Paediatric Plans (PIPs and PSPs)
- Q&A documents
- Device Documents: CIPs, CIRs, and CERs
Our publication experts help you create awareness of your results, innovations, and discoveries in the scientific community.
We support the development of a wide range of scientific and medical publications, including:
- Manuscripts for peer-reviewed journals
- Systematic literature reviews and meta-analyses
- Conference abstracts, posters, and oral presentations
Our expert team brings deep scientific understanding across all phases of clinical development and a broad spectrum of therapeutic areas and product types, including small molecules, recombinant proteins, gene therapies, oncolytic viruses, photodynamic therapy and modified stem cell transplantation.
Check out our expert’s interview!

Why partner with us? Expert 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, Rare Disease and CNS

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.