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.
- 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
- 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
- ・Introduction of Clinical Study-CRC
- ・Practicality in Clinical Study-CRC
- ・GCP Online Test
- ・Introductory Training of a Monitor
【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.
- ・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
- ・Selection of Medical Institutions and Investigators (Surveillance Requirements)
- ・SDV（Source Document Verification) with CRF
- ・Explanatory Meeting for Medical Office
- ・Study Contract Request
- We have practical contents through experienced know-how which are unavailable in other
- Full customized flexible design is feasible.
- 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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