Since its establishment in July 1992, ASKLEP has been providing clinical monitoring services and has nurtured strong relationships and mutual trust with its client pharmaceutical companies, and sponsors.
We have great confidence that this is due to the results we have produced over the last 15 years as a collaborative partner with pharmaceutical companies and medical institutions. From a CRO perspective, this approach achieves efficient pharmaceutical R&D and helps meets stringent timelines.
Working within a corporate policy that our efforts are ultimately intended to benefit patients who are battling disease, illness and injury, ASKLEP continues to provide trusted services to both pharmaceutical companies and medical institutions throughout Japan.
Clinical monitoring expertise
- Establish plans for implementing clinical trials/trial design
- Selection of medical institutes/investigators
- Preparation of manuals, informed consent, case report forms, and others
- Monitoring
- Screening medical institutes / investigators for GCP compliance
- Commission medical institutes, monitoring, and trial termination procedures
- Source data verification (SDV)
