Quintiles.com

  • Japan Clinical Services

  • clinical-trials-header
  • Quintiles Clinical Trial

    The circumstances surrounding healthcare system and clinical trials in Japan have been changing rapidly and dramatically.

    Under such circumstances, it is important for companies that are doing business in Japan to determine what kind of approach they should take for further progress in the future.

    Quintiles is committed to providing high level and quality services to bring your pharmaceutical and medical device business success in the shortest possible time.We review our broad services constantly and strive to make lasting improvements to meet the needs of rapidly changing times.

  • Our Clinical Development Services provides the following services:

    • Clinical trial activities from Phase I through Phase IV
    • Clinical monitoring
    • Data management
    • Statistical analysis & imaging
    • GCP audit, clinical study site audit
    • Support in consultation with Japanese regulatory agency PMDA
    • Regulatory consultation
    • Assistance in safety information management
    • Support in application for approval 
    • MedDRA support and maintenance
    • Medical writing
    • In-Country Clinical Caretaker (ICCC) service
    • Support for multinational study (global study/Asian study) projects
    • Support for simultaneous development in Japan, Europe and the US
    • Clinical trials and related activities outside of Japan
    • PMS (post-marketing surveillance and post-marketing clinical trials)
    • ECG analysis

    We provide solutions customized to the needs of customers to achieve the best possible results in all the above areas.