Clinical Research
idCO provides global clinical trial management services, helping companies and academia develop and implement sustainable research programmes. Whether you're just getting started, or require a site or trial rescue mission, idCO's team of international experts can assist you. Our solution-focused approach reflects our unique combination of clinical trial expertise and practical industry experience.
1) Clinical Trial Management
Listed below are the Clinical Trial Management tools and services with which idCO BV can help you at different phases of the clinical research process:
- Pre-initiation phase
Preparation of clinical trial, data management and statistical analysis plans, medical writing, protocol evaluation, regulatory and ethics approval process, budget and forecast, evaluation of central laboratory and other outsourced services, contract negotiation, case report form design, site preparation. - On-study phase
Study initiation, monitoring, contract management, outsourcing management. - Close-out phase
Data query resolution, preparation of final study reports, preparation for audits, preparation of publication/presentations.
2) Academic Clinical Research Unit Support
In addition to the clinical trial management services listed above, idCO can also provide academic research groups with the following tools and training.
- Infrastructure
- Clinical trial portfolio management
- GCP compliant quality management systems
- Finance
- Project budget preparation and management
- Grant application and submission