Pharmaceutical Research Organization works hand-in-hand with the study sponsor and their representatives, Institutional Review Boards, Investigative Sites, and patients to facilitate a smooth clinical trial process from onset to completion by:
- Identifying Qualified and Experienced Investigative Sites
- Protocol Review and Feasibility Analysis for Investigative Sites
- Recruitment and Training of a Principal Investigator, and any Sub-Investigators
- Recruitment and Training of Ancillary Clinical Staff as appropriate
- Contract and Budget Negotiation
- Regulatory Affairs Management
- Research-Dedicated Study Coordinator
- Placement and Training
- Patient Recruitment and Screening
- Qualified Patient Enrollment and Follow-Up
- Data Collection
- Internal Quality Control
- GCP/ICH Annual Training for Principal Investigators
- Continuing Education
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