VCRO’s services in the United States began in 2009, with services ranging from FDA regulatory representatives and contact window, FDA regulatory consultations, FDA meeting coordinators, FDA IND to NDA submission and regulatory response progress management, FDA response during IND trials, Submission and management of annual trial reports to FDA, investigation and selection of U.S. trial centers and moderators, negotiation of trial center contracts, convening of clinical trial moderator meetings, clinical trial GCP monitoring, trial center management, trial center startup and closure, U.S. vendor management, etc. …;The goal is to support multinational trials of all works in the United States and make it all compliant.

VCRO USA is located in Delaware State and provides customers with 100% CRO service in the United States at all times.

For US business requirements, please contact：

Email：customer@vcro.com.tw
Tel：+886-2-2657-5399#2264
Contact person：Leon Chen

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