IDDI is a Biometrics CRO offering strategic-level consultancy to optimize Biotechs' clinical development program even in clinical trials with complex settings, a Randomization and Trial Supply Management (RTSM) platform and services associated, Clinical Data Management services including EDC systems and SDTM and Biostatistics services including interim and final analyses, IDMC, ISS/ISE, etc.
Based in North Carolina and in Belgium, IDDI has 30 years of experience and has supported 1300 clinical trials so far.
We are working mainly with Biotech companies which have a need to be accompanied along their clinical trial journey starting with trial design until data submission to regulatory authorities.
Our added value is in our rigorous scientific and statistical approach but also our experience dealing closely with FDA and EMA.
75% of our trials are in oncology and ophthalmology but in our 30Y expedience we have touched a lot of other therapeutic areas.
Please pass by our booth or contact us at info@iddi.com
Based in North Carolina and in Belgium, IDDI has 30 years of experience and has supported 1300 clinical trials so far.
We are working mainly with Biotech companies which have a need to be accompanied along their clinical trial journey starting with trial design until data submission to regulatory authorities.
Our added value is in our rigorous scientific and statistical approach but also our experience dealing closely with FDA and EMA.
75% of our trials are in oncology and ophthalmology but in our 30Y expedience we have touched a lot of other therapeutic areas.
Please pass by our booth or contact us at info@iddi.com
Focus Areas
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