IDDI is involved in various steps of clinical research, from experimental design to publication and/or submission of trial results for regulatory approval.
The chart below outlines the steps in designing, conducting, analyzing and reporting clinical trials. It shows IDDI services and tools.
- Drug Screening - Animal Models
- Epidemiologic Studies
- Clinical Development Plan
- Protocol Development
- Experimental Design
- Choice of Endpoints
- Site Selection
- Ethical Approval
- Investigational Brochure
- Case Report Form
- Pre-Clinical Development
- Trial Design
- Trial Implementation
- Patient Screening
- Patient Treatment
- Trial Monitoring and Coordination
- Clinical and non Clinical Observations
- Data Validation
- Reporting of Adverse Events
- Plan
- Interim Statistical Analysis
- Final Statistical Analysis
- Presentations at Conferences
- Meta-Analyses
- Study Reports and Publications
- Submission to Agencies
- Evidence-based Medicine