By Utilizing e-Learning and Classroom Learning with Experienced Know-How in Clinical Study, We Perform Practical and Workable Services

Based on experienced know-how in CRO, we provide effective uniform education and training services via e-learning and practical classroom lectures by clinical development specialist. We also provide practical and workable training system to reduce cost and time which has already been proven in our company.

e-Learning

【Benefits】

  • Reducing cost and time to find lectures and locations
  • Computerized training materials
  • Homogeneous human resources
  • Realization of One-to-One training
  • Re-use of existent lecturers
  • Speed-up of the training by simultaneous education
  • Clear evaluation

e-Learning

  • Easy to use even for internet beginners
  • Easy to manage of lecture records and scores
  • Real-time discussion is possible via email and bulletin board
  • Mentoring supports by lecturers
  • Practical contents by utilizing CRO experience in clinical study
  • Online test, immediate scoring and evaluation are available
  • Customized lecture is provided upon your request
●Lectures
・Introduction of Clinical Study-CRC
・Practicality in Clinical Study-CRC
・GCP Online Test
・Introductory Training of a Monitor

Classroom Learning

【Introductory Training of a Monitor（CRA）】

  • Monitors are required not only knowledge of regulatory requirements of GCP and logical way of thinking but also need communication skill with client and persons involved in the clinical study.
  • We have 3-week basic training in how to be a professional monitor.
  • Lecturers have clinical development experience in pharmaceutical companies or leaders of monitoring at present.
  • We provide role-playing to experience communication with investigators or coordinators involved in the study.

●Lectures
・Introduction of Clinical Study　
・Clinical Study Algorithm and Organization
・Monitoring-Related Regulation
・GCP Guideline
・Investigator’s Brochure
・Protocol and CRF
・Briefing on Informed Consent
・Clinical Study Budget
・Insurance and Compensation
・Collection of Pharmacovigilance Data
●Role-playing
・Selection of Medical Institutions and Investigators (Surveillance Requirements)
・SDV（Source Document Verification) with CRF
・Explanatory Meeting for Medical Office
・Study Contract Request

  1. We have practical contents through experienced know-how which are unavailable in other company.
  2. Full customized flexible design is feasible.
  3. We are able to provide any kind of e-learning and lectures to all members who work in clinical study.

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

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