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?

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

Insights

Utilising CROs for Effective Planning and Execution of Clinical Development

At the recent BioStock Summit in Lund, Aixial’s experts, Ashley Hunter, Senior Director of Clinical Operations and Head of Strategic Development & Delivery, and Anna Yanaeva, Senior Director for Business Development, led an engaging discussion on the importance of “Utilising CROs for Effective Planning and Execution of Clinical Development”.

Writings with molecules and standards as main characters

Clear communication is essential to drug development. At Aixial Group, our experienced medical writers know how to turn complex scientific data into clear, accurate documents. From regulatory protocols to scientific publications, they ensure clarity and compliance at every stage.

Clinical trials – when digital becomes critical

Digitalisation — Clinical trials are essential research studies evaluating medical intervention safety and efficacy, with varying designs and phases aimed at understanding treatment effects and patient experiences…

Atomising cancer

Breakthrough — Radiopharmaceutical therapy represents a novel approach to treating cancer, utilising radioactive atoms to target and destroy malignant cells with precision, without affecting the patient’s healthy tissues. A field in which Aixial has emerged as a pioneer.

Training and upskilling are part of our genes

Talents — The world of life sciences is vast and constantly evolving. It’s not enough to follow trends: you have to anticipate them, and to do that you need to bring together the best specialists. At Aixial Group, Stéphane Thérèse is well aware of this.

OTHER WAYS WE SUPPORT YOU

Helping you succeed in your project

Biostatistical

Clinical data management

Pharmacovigilance