We have developed a strong reputation for delivering a high quality, reliable and responsive medical writing service.
Our dedicated team of professional medical writers provides a complete writing service to clients around the globe, from the generation of individual documents to extensive medical writing programs.
You can rely on our experts to prepare, research, edit or proof copy for a wide range of documents required for the smooth running 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 clinical trial.
We can also offer general medical communications such as publications, posters, abstracts, and promotional and educational material.
All documents are tailored to your individual requirements and produced to the applicable regulatory guidelines.
The medical writing team works closely with key operational departments – Medical, Clinical, Pharmacy and Regulatory Affairs, Statistics and Data Management, Project Management, Quality Assurance and Bioanalytical in order to access a fully-integrated network of expertise as appropriate for your project.