IDDI
Information
IDDI – Patient-Focused, Data-Driven Regulatory Partner
Founded in 1991, IDDI (International Drug Development Institute) is a trusted partner for pharmaceutical, biotechnology, and medical device companies worldwide. With over 35 years of expertise, 350+ clients, and involvement in more than 1,445 clinical trials, we specialize in solving complex data challenges to ensure clinical data is ready for regulatory submission.
Our mission is to challenge the status quo in clinical development by delivering innovative, compliant, and patient-focused solutions that accelerate approvals and enhance trial success.
Our Services:
- Clinical Development Strategy
- Regulatory Statistics & Trial Optimization
- Clinical Trial Design
- Randomization & Trial Supply Management (RTSM)
- Clinical Data Management - EDC
- Biostatistics & Independent Data Monitoring Committees (IDMC)
Why Choose IDDI
- Approval-Optimizing Strategies : Expert regulatory statistics to optimize your clinical development and accelerate approvals.
- Seamless Data Integration : Collaboration between RTSM, Clinical Data Management, and Biostatistics at every step for faster, high-integrity data and results.
- Experienced & Committed Team : Highly skilled staff with exceptional retention rates, ensuring continuity, efficiency, and direct access to executive management.
- Agile & Collaborative Approach : Established partnerships with regulatory authorities and clinical CROs, enabling IDDI to act as an extension of the Sponsor when needed.
- Innovation in R&D –: Pioneering trial designs, novel endpoints, and advanced clinical development strategies for complex studies.