ARIANNE provides a wide range of medical writing services for all phases of the clinical trial process. ARIANNE’s Medical writing team consists of highly knowledgeable individuals with various advanced degrees, a wide range of clinical research experience and extensive knowledge of the clinical, biostatistics, and regulatory processes.
ARIANNE provides the following services:
- Protocol development, review and update
- Investigator's Brochure (IB) and IB amendments
- Development of Informed Consent
- Medical and safety report writing
- Development of operation manuals
- Planning and writing of summary documents
- Study summary reports (preparation, review and submissions)