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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
    • Investigators 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)