Research & Development is the Integral part of Ceyon, we are systematically develop a new technology platforms in Clinical food research and products development. we also doing research in linking the areas of Agriculture biotechnology, medical food and chronotherpeutics,
Clinical trial management and provides clients with highly trained study teams. These teams include a Clinical Research Associates (CRAs), and In-House CRAs who ensure successful project . Using a risk-based approach to site monitoring we ensure that the participant rights are protected, the data are accurate and complete, and the project is completed on time and within budget.
- Investigator identification and selection
- Institutional Review Board and Ethics Committee approval coordination
- Investigator contracts negotiation
- Development of Monitoring Plans and Manuals of Procedures (MOPS)
- Initial collection and review of essential documents
- Design and implementation of recruitment strategies
- Ongoing Activities
- Site payments
- Design and implementation of patient retention strategies
- Continuous training and support to address site staff turnover and deficiencies noted during monitoring
- Clinical Site Monitoring Services
- Site assessment and activation
- Training
- Patient recruitment and community outreach
- Monitoring of recruitment, eligibility, and informed consent procedures
- Source Data Verification
- Review of Investigational Product and accountability records
- Review of compliance with Adverse Events reporting requirements
- In-House Site Management
- Remote monitoring of regulatory files
- Site queries resolution
PROJECT MANAGEMENT AND REPORT WRITING
- Clinical Development Phase I-IV
- Protocols
- Informed Consents and appropriate translations
- Clinical Study Reports
- Post-Marketing
- Abstracts and manuscripts
- Design and management of REMS (Risk Evaluation and Mitigation Strategies)
