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)