ICBIO offers a full range of clinical drug development services worldwide.

We have a successful track record of managing programs in all phases of clinical development. ICBIO distinguishes itself by having facilities inside hospitals to allow rapid recruitment of patients and volunteers. In Phase II-III, ICBIO has executed many pivotal trials that led to FDA and/or international regulatory approval. In late phase, we assist clients with the post-approval process by planning and conducting large, simple studies, registries, outcome studies, and risk management programs.

Choosing an appropriate partner for the drug development process is the most critical step in Clinical Research. ICBio provides professional, innovative, effective and most comprehensive clinical trial solutions for the needs of pharmaceutical, biotechnology and other Healthcare industries globally in their clinical development by evolving various strategies to ensure timely execution of clinical projects and cost-competitive services.

ICBio is a lucrative ‘One Point Contact’ for all clinical research requirements.

Our comprehensive services include: