IDDI, Your eClinical and Biostatistical Services Provider since 1991

Trial Design .  Randomization  ·  Data Management  ·  Biostatistics

 
 

  • 500+ Phase I-IV trials                         
  • Regulatory experience with involvement in 15 FDA/EMA approvals
  • Multiple areas of expertise including:
    Oncology, ophthalmology, cardiology, infectious diseases, immunology.

How does IDDI add value to Clinical Data?

  • Because of the nature of its activity and focus on specialized services, IDDI is uniquely positioned to add value by planning, collecting, managing, analyzing and reporting clinical data.
  • IDDI offers high value services in trial design, data management, including EDC, biostatistical analyses and medical writing.
  • IDDI has developed highly innovative web systems to optimize clinical research, such as IWRS (Interactive Web Response System) (IVRS Interactive Voice Response System also available) and a medical coding system.  

">">"> 

IDDI Bay Area Complimentary Seminar           REGISTER HERE

SMARTER CLINICAL TRIALS - GAINING TIME WITHOUT INCREASING RISK

March 8, 2012, from 7:00 am to 1:30 pm  - Menlo Park, CA

The purpose of this Seminar is to outline recent developments in trial design and statistical methodology that will enable participants to address these challenges effectively. The four sessions will mix of statistical theory and application to actual trials, including a discussion of success and failure stories.
Speakers : Dr. Marc Buyse, ScD, Chairman IDDI - Dr Jay Herson, PhD, Johns Hopkins Bloomberg School of Public Health.