Virginia Contract Research Organization Co., Ltd. (VCRO), a CRO hosted in Taiwan, was founded on July 21st 1997. In Taiwan, VCRO is a most experienced and historic contract research organization (CRO) specializing in variety of clinical services. We implement clinical trials related service in compliance with the guidance of International Conference on Harmonisation (ICH). In order to further provide comprehensive service in the area of drug developments, VCRO established a bioanalytical laboratory (BioLab) in the spring of 2002. Therefore, VCRO is a solution provider which comprehensively handles BA / BE studies of generic drugs and clinical trials of investigational new drugs (IND) from Phase I to III as well as clinical researches in Phase IV, after new drug application (NDA).
VCRO has been in the market for more than 21 years, incorporating a full service range from IND to NDA. In addition to clinical trial services, we also have EDC, IVR, and IWR, and OECD-accredited GLP bioanalytical laboratory. Our in-house medical writing service also have excellent experience in a few US FDA IND writing and submissions with continuing successes. In recent years, we have transformed from participation to LEAD on US-FDA IND studies. VCRO is confident to take your order in your coming requests.