I provide specialised medical writing support to organisations and professionals involved in clinical research, pharmaceutical development and medical device development.
I work with different types of clients, adapting my support to their project requirements, documentation needs and regulatory context.
CROs (Contract Research Organisations)
I provide medical writing support to CROs involved in the planning, conduct and reporting of clinical trials. I can support project teams with the preparation, review and updating of clinical and regulatory documentation, helping to meet project timelines and documentation requirements.
Pharmaceutical & Biotechnology Companies
I support pharmaceutical and biotechnology companies in the development of clear, accurate and scientifically sound documentation throughout the drug development process. My services include the preparation and review of clinical and regulatory documents supporting clinical development and regulatory submissions.
Clinical Trial Sponsors
I provide medical writing support to clinical trial sponsors throughout the clinical development process, from protocol development to clinical study reporting. I help ensure that documentation is scientifically accurate, consistent and aligned with applicable regulatory requirements.
Clinical Researchers & Investigators
I support clinical researchers and investigators with the preparation and development of clinical research documentation. This includes protocols, study-related documents and scientific content, with an emphasis on clarity, accuracy and consistency.
Medical Device Manufacturers
I support medical device manufacturers with the preparation and development of clinical and regulatory documentation related to clinical investigations and clinical evaluation, in accordance with applicable medical device requirements.
Let’s Discuss Your Project
Whether you need support with a specific document or ongoing medical writing assistance, I would be happy to discuss your requirements.