Our team of professional medical writers provides a complete writing service to clients around the globe.
Our medical writing team works closely with key operational departments – Medical, Clinical, Pharmacy, Regulatory Affairs, Biostatistics, Data Management, Project Management, Quality Assurance, and Bioanalysis — in order to access a fully-integrated network of expertise.
You can rely on our dedicated experts to prepare, research, edit, or proof copy for a wide range of documents required for the smooth conduct of your trial, including:
- Protocol amendments
- Informed Consent Forms
- Clinical study reports
- Pharmacokinetic reports
- Biostatistical reports
- Bioanalytical reports
- Safety reports
- Any other type of document necessary for a successful trial
We also offer general medical communications services, on behalf of sponsors, including publications, posters, abstracts, and promotional and educational material.
All documents are tailored to your individual requirements and produced in accordance with relevant regulatory guidelines.