Evaluating and Verifying Clinical Trials from an Independent Standpoint

GCP auditing operations are conducted as part of quality assurance activities in order to improve the reliability of a clinical trial by evaluating and verifying, whether the clinical trial is conducted in compliance with GCP (GPSP), Pharmaceutical Affairs Law, protocol, and standard operating procedures, etc.

work flow

Major Services

  • Consultation in accordance with GCP, Related Laws, Regulations and Standards
  • System Audits
  • Audit of Medical Institutions Conducting Clinical Trials
  • Internal and External Audits of Individual Contract Services
  • Audit Investigator initiated Clinical Trials

  1. Our staff, well versed in the concepts of ISO9000 and familiar with clinical trials, are actively engaged.
  2. Our staff, experienced in audit activities in pharmaceutical companies and other organization, conduct efficient and high quality audits.
  3. Our staff, with high level of communication skills, attend to various requirements appropriately.
  4. We provide services with aiming towards continual improvement.

[ Contact ] Sales Department TEL +81-3-5804-7577 / FAX +81-3-5684-7872

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